MICAL2[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 144515	GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3	TRIM22, TRIM3 +917 more	Copy number gain	See cases	GPathogenic
Select item 147607	GRCh38/hg38 11p15.4-15.2(chr11:9989516-16825806)x1	BMAL1, BTBD10 +208 more	Copy number loss	See cases	GPathogenic
Select item 57271	GRCh38/hg38 11p15.3(chr11:12147544-12638655)x3	LOC112042781, LOC112042782 +8 more	Copy number gain	See cases	GUncertain significance
Select item 2209423	NM_001282663.2(MICAL2):c.8A>T (p.Glu3Val)	MICAL2 (E3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269920	NM_001282663.2(MICAL2):c.15G>C (p.Glu5Asp)	MICAL2 (E5D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617873	NM_001282663.2(MICAL2):c.19G>A (p.Glu7Lys)	MICAL2 (E7K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294747	NM_001282663.2(MICAL2):c.31C>A (p.Gln11Lys)	MICAL2 (Q11K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251102	NM_001282663.2(MICAL2):c.83C>G (p.Thr28Ser)	MICAL2 (T28S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126137	NM_001282663.2(MICAL2):c.120C>A (p.Asp40Glu)	MICAL2 (D40E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 786189	NM_001282663.2(MICAL2):c.121C>G (p.Leu41Val)	MICAL2 (L41V)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2378065	NM_001282663.2(MICAL2):c.130C>G (p.Leu44Val)	MICAL2 (L44V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2368247	NM_001282663.2(MICAL2):c.215G>A (p.Arg72His)	MICAL2 (R72H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2486334	NM_001282663.2(MICAL2):c.225C>A (p.His75Gln)	MICAL2 (H75Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524892	NM_001282663.2(MICAL2):c.260C>A (p.Thr87Asn)	MICAL2 (T87N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126169	NM_001282663.2(MICAL2):c.271A>C (p.Ile91Leu)	MICAL2 (I91L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324666	NM_001282663.2(MICAL2):c.271A>T (p.Ile91Leu)	MICAL2 (I91L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2311192	NM_001282663.2(MICAL2):c.317C>A (p.Ala106Asp)	MICAL2 (A106D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257957	NM_001282663.2(MICAL2):c.340G>A (p.Val114Met)	MICAL2 (V114M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331179	NM_001282663.2(MICAL2):c.410T>A (p.Leu137His)	MICAL2 (L137H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218309	NM_001282663.2(MICAL2):c.464A>G (p.Asp155Gly)	MICAL2 (D155G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126184	NM_001282663.2(MICAL2):c.514A>T (p.Met172Leu)	MICAL2 (M172L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3294750	NM_001282663.2(MICAL2):c.601C>T (p.Arg201Trp)	MICAL2 (R201W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126185	NM_001282663.2(MICAL2):c.617C>T (p.Pro206Leu)	MICAL2 (P206L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2324814	NM_001282663.2(MICAL2):c.656T>C (p.Ile219Thr)	MICAL2 (I219T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126187	NM_001282663.2(MICAL2):c.719A>T (p.Lys240Met)	MICAL2 (K240M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126189	NM_001282663.2(MICAL2):c.767C>T (p.Ala256Val)	MICAL2 (A256V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545362	NM_001282663.2(MICAL2):c.814C>G (p.Gln272Glu)	MICAL2 (Q272E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294732	NM_001282663.2(MICAL2):c.865A>G (p.Ile289Val)	MICAL2 (I289V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294743	NM_001282663.2(MICAL2):c.890A>G (p.His297Arg)	MICAL2 (H297R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294738	NM_001282663.2(MICAL2):c.928G>A (p.Asp310Asn)	MICAL2 (D310N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378594	NM_001282663.2(MICAL2):c.935G>A (p.Gly312Asp)	MICAL2 (G312D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384128	NM_001282663.2(MICAL2):c.949G>C (p.Asp317His)	MICAL2 (D317H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364355	NM_001282663.2(MICAL2):c.980C>T (p.Ala327Val)	MICAL2 (A327V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126133	NM_001282663.2(MICAL2):c.1018C>T (p.Arg340Trp)	MICAL2 (R340W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350935	NM_001282663.2(MICAL2):c.1019G>A (p.Arg340Gln)	MICAL2 (R340Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126135	NM_001282663.2(MICAL2):c.1135A>T (p.Asn379Tyr)	MICAL2 (N379Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2221645	NM_001282663.2(MICAL2):c.1151G>A (p.Arg384Gln)	MICAL2 (R384Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2641609	NM_001282663.2(MICAL2):c.1206+4C>T	MICAL2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3126138	NM_001282663.2(MICAL2):c.1238G>A (p.Arg413His)	MICAL2 (R413H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294748	NM_001282663.2(MICAL2):c.1270A>G (p.Met424Val)	MICAL2 (M424V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126140	NM_001282663.2(MICAL2):c.1280G>A (p.Ser427Asn)	MICAL2 (S427N)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2604621	NM_001282663.2(MICAL2):c.1287C>A (p.Asn429Lys)	MICAL2 (N429K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550119	NM_001282663.2(MICAL2):c.1306G>A (p.Glu436Lys)	MICAL2 (E436K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212731	NM_001282663.2(MICAL2):c.1358C>T (p.Pro453Leu)	MICAL2 (P453L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294736	NM_001282663.2(MICAL2):c.1508C>T (p.Ser503Leu)	MICAL2 (S503L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510274	NM_001282663.2(MICAL2):c.1560C>A (p.Ser520Arg)	MICAL2 (S520R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2510276	NM_001282663.2(MICAL2):c.1561A>G (p.Lys521Glu)	MICAL2 (K521E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601118	NM_001282663.2(MICAL2):c.1618G>A (p.Asp540Asn)	MICAL2 (D540N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210907	NM_001282663.2(MICAL2):c.1630T>A (p.Ser544Thr)	MICAL2 (S544T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273051	NM_001282663.2(MICAL2):c.1637G>A (p.Arg546His)	MICAL2 (R546H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377593	NM_001282663.2(MICAL2):c.1675C>T (p.Arg559Trp)	MICAL2 (R559W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 789311	NM_001282663.2(MICAL2):c.1676G>A (p.Arg559Gln)	MICAL2 (R559Q)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2332676	NM_001282663.2(MICAL2):c.1712A>G (p.Asp571Gly)	MICAL2 (D571G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294729	NM_001282663.2(MICAL2):c.1757G>A (p.Arg586Gln)	MICAL2 (R586Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126148	NM_001282663.2(MICAL2):c.1822C>T (p.Leu608Phe)	MICAL2 (L608F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2471123	NM_001282663.2(MICAL2):c.1831G>T (p.Val611Phe)	MICAL2 (V611F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126151	NM_001282663.2(MICAL2):c.1868G>T (p.Gly623Val)	MICAL2 (G623V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126152	NM_001282663.2(MICAL2):c.1870A>T (p.Thr624Ser)	MICAL2 (T624S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2540980	NM_001282663.2(MICAL2):c.1885G>A (p.Val629Met)	MICAL2 (V629M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 779350	NM_001282663.2(MICAL2):c.1907A>G (p.Tyr636Cys)	MICAL2 (Y636C)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3126155	NM_001282663.2(MICAL2):c.1952A>G (p.Asn651Ser)	MICAL2 (N651S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126157	NM_001282663.2(MICAL2):c.1966C>T (p.Leu656Phe)	MICAL2 (L656F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294735	NM_001282663.2(MICAL2):c.1985G>A (p.Arg662Lys)	MICAL2 (R662K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208559	NM_001282663.2(MICAL2):c.1993C>T (p.Arg665Trp)	MICAL2 (R665W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620849	NM_001282663.2(MICAL2):c.2033G>A (p.Arg678Gln)	MICAL2 (R678Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457724	NM_001282663.2(MICAL2):c.2050A>G (p.Thr684Ala)	MICAL2 (T684A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235877	NM_001282663.2(MICAL2):c.2135A>C (p.Gln712Pro)	MICAL2 (Q712P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126160	NM_001282663.2(MICAL2):c.2189C>T (p.Thr730Ile)	MICAL2 (T730I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3126161	NM_001282663.2(MICAL2):c.2191C>T (p.Arg731Trp)	MICAL2 (R731W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294733	NM_001282663.2(MICAL2):c.2192G>A (p.Arg731Gln)	MICAL2 (R731Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241441	NM_001282663.2(MICAL2):c.2198C>T (p.Pro733Leu)	MICAL2 (P733L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3294745	NM_001282663.2(MICAL2):c.2216A>G (p.Glu739Gly)	MICAL2 (E739G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126162	NM_001282663.2(MICAL2):c.2218C>T (p.Arg740Cys)	MICAL2 (R740C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2459672	NM_001282663.2(MICAL2):c.2219G>A (p.Arg740His)	MICAL2 (R740H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2641610	NM_001282663.2(MICAL2):c.2262C>T (p.Ser754=)	MICAL2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2384836	NM_001282663.2(MICAL2):c.2357C>T (p.Thr786Met)	MICAL2 (T786M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2246439	NM_001282663.2(MICAL2):c.2483C>G (p.Ser828Cys)	MICAL2 (S828C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3294749	NM_001282663.2(MICAL2):c.2488C>A (p.Arg830Ser)	MICAL2 (R830S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126163	NM_001282663.2(MICAL2):c.2524C>T (p.Arg842Trp)	MICAL2 (R842W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2515550	NM_001282663.2(MICAL2):c.2525G>A (p.Arg842Gln)	MICAL2 (R842Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126164	NM_001282663.2(MICAL2):c.2531A>G (p.Gln844Arg)	MICAL2 (Q844R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2513476	NM_001282663.2(MICAL2):c.2541G>T (p.Glu847Asp)	MICAL2 (E847D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2529563	NM_001282663.2(MICAL2):c.2542G>C (p.Glu848Gln)	MICAL2 (E848Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2507512	NM_001282663.2(MICAL2):c.2563G>A (p.Ala855Thr)	MICAL2 (A855T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2322232	NM_001282663.2(MICAL2):c.2609A>G (p.Glu870Gly)	MICAL2 (E870G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2401776	NM_001282663.2(MICAL2):c.2615C>T (p.Ala872Val)	MICAL2 (A872V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2349794	NM_001282663.2(MICAL2):c.2632A>T (p.Met878Leu)	MICAL2 (M878L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126167	NM_001282663.2(MICAL2):c.2654C>T (p.Pro885Leu)	MICAL2 (P885L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126168	NM_001282663.2(MICAL2):c.2687A>G (p.His896Arg)	MICAL2 (H896R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2218010	NM_001282663.2(MICAL2):c.2689A>G (p.Thr897Ala)	MICAL2 (T897A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126170	NM_001282663.2(MICAL2):c.2740T>G (p.Ser914Ala)	MICAL2 (S914A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2357175	NM_001282663.2(MICAL2):c.2797C>T (p.Pro933Ser)	MICAL2 (P933S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3294744	NM_001282663.2(MICAL2):c.2804G>C (p.Gly935Ala)	MICAL2 (G935A +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126171	NM_001282663.2(MICAL2):c.2804G>T (p.Gly935Val)	MICAL2 (G935V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3126173	NM_001282663.2(MICAL2):c.2818C>T (p.Pro940Ser)	MICAL2 (P750S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3294734	NM_001282663.2(MICAL2):c.2840A>G (p.His947Arg)	MICAL2 (H947R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2539016	NM_001282663.2(MICAL2):c.2849T>G (p.Leu950Arg)	MICAL2 (L929R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2272087	NM_001282663.2(MICAL2):c.2872G>A (p.Gly958Arg)	MICAL2 (G937R +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2301031	NM_001282663.2(MICAL2):c.2903A>G (p.Asn968Ser)	MICAL2 (N778S +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2539828	NM_001282663.2(MICAL2):c.2951A>G (p.Asp984Gly)	MICAL2 (D794G +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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