Related gene-specific medical variations for Gene (Select 6335) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3247364	NC_000002.11:g.(?_167136847)_(167168266_?)dup	SCN9A	Duplication	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 3236177	NM_001365536.1(SCN9A):c.5060G>A (p.Ser1687Asn)	SCN1A-AS1, SCN9A (S1676N +1 more)	Single nucleotide variant (missense variant)	Primary erythromelalgia	GUncertain significance
Select item 3158580	NM_001365536.1(SCN9A):c.5278C>A (p.Leu1760Met)	SCN1A-AS1, SCN9A (L1749M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3158577	NM_001365536.1(SCN9A):c.3010C>G (p.Gln1004Glu)	SCN1A-AS1, SCN9A (Q993E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3158575	NM_001365536.1(SCN9A):c.1120G>T (p.Ala374Ser)	SCN1A-AS1, SCN9A (A374S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3064178	NM_001365536.1(SCN9A):c.3536G>A (p.Trp1179Ter)	SCN1A-AS1, SCN9A (W1168* +1 more)	Single nucleotide variant (nonsense)	Channelopathy-associated congenital insensitivity to pain, autosomal recessive	GPathogenic
Select item 3063713	NM_001365536.1(SCN9A):c.1415G>T (p.Ser472Ile)	SCN1A-AS1, SCN9A (S472I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3061499	NM_001365536.1(SCN9A):c.3180T>C (p.Ser1060=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	SCN9A-related disorder	GLikely benign
Select item 3049456	NM_001365536.1(SCN9A):c.1974+9_1974+15del	SCN1A-AS1, SCN9A	Deletion (intron variant)	SCN9A-related disorder	GLikely benign
Select item 3041636	NM_001365536.1(SCN9A):c.1974+9G>A	SCN9A, SCN1A-AS1	Single nucleotide variant (intron variant)	SCN9A-related disorder	GBenign
Select item 2954532	NM_001365536.1(SCN9A):c.5401A>G (p.Lys1801Glu)	SCN1A-AS1, SCN9A (K1790E +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954519	NM_001365536.1(SCN9A):c.3979G>T (p.Val1327Leu)	SCN1A-AS1, SCN9A (V1327L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954386	NM_001365536.1(SCN9A):c.993G>T (p.Val331=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954382	NM_001365536.1(SCN9A):c.5185G>A (p.Asp1729Asn)	SCN1A-AS1, SCN9A (D1729N +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954372	NM_001365536.1(SCN9A):c.3430G>A (p.Glu1144Lys)	SCN1A-AS1, SCN9A (E1144K +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954209	NM_001365536.1(SCN9A):c.3724C>G (p.Leu1242Val)	SCN1A-AS1, SCN9A (L1231V +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954118	NM_001365536.1(SCN9A):c.2343+16T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2954115	NM_001365536.1(SCN9A):c.1047G>C (p.Trp349Cys)	SCN1A-AS1, SCN9A (W349C)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2954073	NM_001365536.1(SCN9A):c.4911G>A (p.Leu1637=)	SCN1A-AS1, SCN9A	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2954032	NM_001365536.1(SCN9A):c.3129T>G (p.Leu1043=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2953978	NM_001365536.1(SCN9A):c.5196C>G (p.Asn1732Lys)	SCN1A-AS1, SCN9A (N1721K +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2953870	NM_001365536.1(SCN9A):c.1635T>C (p.Ser545=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2953710	NM_001365536.1(SCN9A):c.2517+12C>T	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2953346	NM_001365536.1(SCN9A):c.5616T>C (p.Pro1872=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2953189	NM_001365536.1(SCN9A):c.2069T>C (p.Met690Thr)	SCN1A-AS1, SCN9A (M679T +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2953061	NM_001365536.1(SCN9A):c.5408C>T (p.Ser1803Phe)	SCN1A-AS1, SCN9A (S1792F +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2952989	NM_001365536.1(SCN9A):c.4493C>T (p.Pro1498Leu)	SCN1A-AS1, SCN9A (P1487L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2952949	NM_001365536.1(SCN9A):c.1344_1345dup (p.Ser449fs)	SCN1A-AS1, SCN9A (S449fs)	Duplication (frameshift variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GPathogenic
Select item 2952931	NM_001365536.1(SCN9A):c.4261-17T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2952927	NM_001365536.1(SCN9A):c.5309G>C (p.Ser1770Thr)	SCN1A-AS1, SCN9A (S1759T +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2952669	NM_001365536.1(SCN9A):c.4788T>A (p.Ala1596=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2952635	NM_001365536.1(SCN9A):c.1797C>A (p.Ser599Arg)	SCN1A-AS1, SCN9A (S599R)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2952553	NM_001365536.1(SCN9A):c.4887G>T (p.Gly1629=)	SCN1A-AS1, SCN9A	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2952498	NM_001365536.1(SCN9A):c.5232CAT[1] (p.Ile1746del)	SCN1A-AS1, SCN9A (I1746del +1 more)	Microsatellite (inframe_deletion +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2952429	NM_001365536.1(SCN9A):c.2247A>C (p.Ala749=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2952426	NM_001365536.1(SCN9A):c.4503+14T>C	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2952363	NM_001365536.1(SCN9A):c.3884del (p.Ala1294_Leu1295insTer)	SCN1A-AS1, SCN9A	Deletion (nonsense +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GPathogenic
Select item 2952247	NM_001365536.1(SCN9A):c.4877G>A (p.Gly1626Glu)	SCN1A-AS1, SCN9A (G1626E +1 more)	Single nucleotide variant (missense variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951870	NM_001365536.1(SCN9A):c.4270C>A (p.Gln1424Lys)	SCN1A-AS1, SCN9A (Q1413K +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951793	NM_001365536.1(SCN9A):c.5687T>C (p.Ile1896Thr)	SCN1A-AS1, SCN9A (I1885T +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951779	NM_001365536.1(SCN9A):c.3386C>G (p.Thr1129Arg)	SCN1A-AS1, SCN9A (T1118R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951773	NM_001365536.1(SCN9A):c.1076C>G (p.Thr359Ser)	SCN1A-AS1, SCN9A (T359S)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951681	NM_001365536.1(SCN9A):c.5566A>G (p.Met1856Val)	SCN1A-AS1, SCN9A (M1856V +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951673	NM_001365536.1(SCN9A):c.5763C>T (p.Asp1921=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2951630	NM_001365536.1(SCN9A):c.3131C>A (p.Ala1044Asp)	SCN1A-AS1, SCN9A (A1033D +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2951201	NM_001365536.1(SCN9A):c.2875-12A>T	SCN9A, SCN1A-AS1	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2951110	NM_001365536.1(SCN9A):c.5440C>T (p.Leu1814Phe)	SCN1A-AS1, SCN9A (L1814F +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950635	NM_001365536.1(SCN9A):c.4774+12T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2950634	NM_001365536.1(SCN9A):c.4774+13_4774+16del	SCN9A, SCN1A-AS1	Microsatellite (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2950616	NM_001365536.1(SCN9A):c.2343+13T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2950481	NM_001365536.1(SCN9A):c.1712C>T (p.Ala571Val)	SCN1A-AS1, SCN9A (A571V)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950417	NM_001365536.1(SCN9A):c.3581T>C (p.Phe1194Ser)	SCN1A-AS1, SCN9A (F1194S +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950314	NM_001365536.1(SCN9A):c.1330G>A (p.Ala444Thr)	SCN1A-AS1, SCN9A (A444T)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950249	NM_001365536.1(SCN9A):c.4155G>A (p.Leu1385=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2950135	NM_001365536.1(SCN9A):c.2684G>A (p.Cys895Tyr)	SCN1A-AS1, SCN9A (C884Y +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950133	NM_001365536.1(SCN9A):c.3336T>A (p.Ser1112Arg)	SCN1A-AS1, SCN9A (S1112R +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2950123	NM_001365536.1(SCN9A):c.2532G>A (p.Lys844=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2950033	NM_001365536.1(SCN9A):c.3013A>G (p.Thr1005Ala)	SCN1A-AS1, SCN9A (T994A +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949956	NM_001365536.1(SCN9A):c.3924+12C>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2949927	NM_001365536.1(SCN9A):c.919G>A (p.Glu307Lys)	SCN1A-AS1, SCN9A (E307K)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949909	NM_001365536.1(SCN9A):c.1018G>T (p.Gly340Cys)	SCN1A-AS1, SCN9A (G340C)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949826	NM_001365536.1(SCN9A):c.5964dup (p.Ter1989IleextTer?)	SCN1A-AS1, SCN9A	Duplication (frameshift variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949616	NM_001365536.1(SCN9A):c.1602+17T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2949605	NM_001365536.1(SCN9A):c.3215A>G (p.Glu1072Gly)	SCN1A-AS1, SCN9A (E1061G +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949520	NM_001365536.1(SCN9A):c.2154A>G (p.Ala718=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2949445	NM_001365536.1(SCN9A):c.1831A>G (p.Met611Val)	SCN1A-AS1, SCN9A (M611V)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949422	NM_001365536.1(SCN9A):c.4279T>G (p.Tyr1427Asp)	SCN1A-AS1, SCN9A (Y1416D +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949362	NM_001365536.1(SCN9A):c.3461G>T (p.Cys1154Phe)	SCN1A-AS1, SCN9A (C1154F +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949338	NM_001365536.1(SCN9A):c.902-6C>T	SCN1A-AS1, SCN9A	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2949327	NM_001365536.1(SCN9A):c.4261-15T>A	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2949263	NM_001365536.1(SCN9A):c.5917A>G (p.Arg1973Gly)	SCN1A-AS1, SCN9A (R1973G +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2949122	NM_001365536.1(SCN9A):c.911A>G (p.Tyr304Cys)	SCN1A-AS1, SCN9A (Y304C)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948996	NM_001365536.1(SCN9A):c.5777T>C (p.Leu1926Ser)	SCN1A-AS1, SCN9A (L1926S +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948989	NM_001365536.1(SCN9A):c.2356A>G (p.Ile786Val)	SCN1A-AS1, SCN9A (I786V +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948952	NM_001365536.1(SCN9A):c.4024T>G (p.Leu1342Val)	SCN1A-AS1, SCN9A (L1331V +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948522	NM_001365536.1(SCN9A):c.4504-27_4504-2dup	SCN1A-AS1, SCN9A	Duplication (splice acceptor variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948504	NM_001365536.1(SCN9A):c.3351+10C>G	SCN1A-AS1, SCN9A	Single nucleotide variant (intron variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2948431	NM_001365536.1(SCN9A):c.4950G>A (p.Leu1650=)	SCN1A-AS1, SCN9A	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2948375	NM_001365536.1(SCN9A):c.5874_5877dup (p.Ser1960Ter)	SCN1A-AS1, SCN9A (S1949* +1 more)	Duplication (nonsense +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948346	NM_001365536.1(SCN9A):c.3165A>C (p.Glu1055Asp)	SCN1A-AS1, SCN9A (E1055D +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948214	NM_001365536.1(SCN9A):c.4775-1G>C	SCN1A-AS1, SCN9A	Single nucleotide variant (splice acceptor variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2948000	NM_001365536.1(SCN9A):c.3385A>C (p.Thr1129Pro)	SCN1A-AS1, SCN9A (T1129P +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947978	NM_001365536.1(SCN9A):c.5410G>A (p.Asp1804Asn)	SCN1A-AS1, SCN9A (D1804N +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947951	NM_001365536.1(SCN9A):c.5918G>T (p.Arg1973Ile)	SCN1A-AS1, SCN9A (R1973I +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947855	NM_001365536.1(SCN9A):c.5635C>G (p.Pro1879Ala)	SCN1A-AS1, SCN9A (P1868A +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947749	NM_001365536.1(SCN9A):c.4551T>A (p.Phe1517Leu)	SCN1A-AS1, SCN9A (F1506L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947660	NM_001365536.1(SCN9A):c.4120A>T (p.Met1374Leu)	SCN1A-AS1, SCN9A (M1363L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2947526	NM_001365536.1(SCN9A):c.3148C>T (p.His1050Tyr)	SCN1A-AS1, SCN9A (H1039Y +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946931	NM_001365536.1(SCN9A):c.4903T>C (p.Phe1635Leu)	SCN1A-AS1, SCN9A (F1635L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946880	NM_001365536.1(SCN9A):c.5378C>A (p.Ala1793Glu)	SCN9A, SCN1A-AS1 (A1782E +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946627	NM_001365536.1(SCN9A):c.5939G>A (p.Gly1980Glu)	SCN1A-AS1, SCN9A (G1969E +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946468	NM_001365536.1(SCN9A):c.3397C>A (p.Pro1133Thr)	SCN1A-AS1, SCN9A (P1133T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946376	NM_001365536.1(SCN9A):c.2072G>A (p.Ser691Asn)	SCN1A-AS1, SCN9A (S680N +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946299	NM_001365536.1(SCN9A):c.5863C>A (p.Pro1955Thr)	SCN1A-AS1, SCN9A (P1955T +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946198	NM_001365536.1(SCN9A):c.5858C>A (p.Thr1953Asn)	SCN1A-AS1, SCN9A (T1953N +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2946073	NM_001365536.1(SCN9A):c.2969T>A (p.Ile990Asn)	SCN1A-AS1, SCN9A (I990N +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2945864	NM_001365536.1(SCN9A):c.4206+2dup	SCN1A-AS1, SCN9A	Duplication (splice donor variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2945846	NM_001365536.1(SCN9A):c.4334C>T (p.Ser1445Leu)	SCN1A-AS1, SCN9A (S1445L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance
Select item 2945831	NM_001365536.1(SCN9A):c.4338C>T (p.Phe1446=)	SCN1A-AS1, SCN9A	Single nucleotide variant (synonymous variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GLikely benign
Select item 2945469	NM_001365536.1(SCN9A):c.5413T>C (p.Phe1805Leu)	SCN1A-AS1, SCN9A (F1794L +1 more)	Single nucleotide variant (missense variant)	Neuropathy, hereditary sensory and autonomic, type 2A +1 more	GUncertain significance

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