ClinVar for Gene (Select 4990) - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 1 to 100 of 143

<< First< Prev

Page of 2

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3369851	NM_007374.3(SIX6):c.359dup (p.Leu121fs)	C14orf39, SIX6 (L121fs)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 3255200	NM_007374.3(SIX6):c.496G>C (p.Gly166Arg)	C14orf39, SIX6 (G166R)	Single nucleotide variant (missense variant)	Colobomatous optic disc-macular atrophy-chorioretinopathy syndrome	GUncertain significance
Select item 3253264	NM_007374.3(SIX6):c.533A>C (p.Asn178Thr)	C14orf39, SIX6 (N178T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3015045	NM_007374.3(SIX6):c.603C>T (p.Ser201=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3006746	NM_007374.3(SIX6):c.432C>T (p.Arg144=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2895297	NM_007374.3(SIX6):c.573-5C>G	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2868886	NM_007374.3(SIX6):c.572+10T>C	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2863514	NM_007374.3(SIX6):c.75C>A (p.Gly25=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2821962	NM_007374.3(SIX6):c.572+8C>T	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2814100	NM_007374.3(SIX6):c.427C>T (p.Leu143=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2794468	NM_007374.3(SIX6):c.327T>C (p.Pro109=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2786995	NM_007374.3(SIX6):c.333C>T (p.Asp111=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2730051	NM_007374.3(SIX6):c.114C>T (p.Pro38=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2729433	NM_007374.3(SIX6):c.279A>G (p.Glu93=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2685487	GRCh37/hg19 14q22.3-23.2(chr14:55667390-64447598)x1	HIF1A, HIF1A-AS2 +47 more	Copy number loss	not provided	GPathogenic
Select item 2684728	GRCh37/hg19 14q23.1-32.33(chr14:58894502-107227240)x3	CCNK, MIR376A1 +353 more	Copy number gain	not provided	GPathogenic
Select item 2684726	GRCh37/hg19 14q22.3-24.1(chr14:57588965-68334517)x3	ACTR10, AKAP5 +71 more	Copy number gain	not provided	GLikely pathogenic
Select item 2684714	GRCh37/hg19 14q11.2-23.1(chr14:20511673-61826023)x3	ABHD12B, ABHD4 +289 more	Copy number gain	not provided	GPathogenic
Select item 2621506	NM_007374.3(SIX6):c.475C>A (p.Arg159Ser)	C14orf39, SIX6 (R159S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2582921	NM_007374.3(SIX6):c.105G>A (p.Trp35Ter)	C14orf39, SIX6 (W35*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 2580623	NM_007374.3(SIX6):c.34C>A (p.Gln12Lys)	C14orf39, SIX6 (Q12K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2548062	NM_007374.3(SIX6):c.124G>A (p.Ala42Thr)	C14orf39, SIX6 (A42T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496480	NM_007374.3(SIX6):c.661A>T (p.Ser221Cys)	C14orf39, SIX6 (S221C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486010	NM_007374.3(SIX6):c.695C>T (p.Thr232Ile)	C14orf39, SIX6 (T232I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480461	NM_007374.3(SIX6):c.155C>G (p.Ser52Trp)	C14orf39, SIX6 (S52W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2425450	NC_000014.8:g.(?_60976117)_(61447691_?)del	MNAT1, SIX1 +3 more	Deletion	not provided	GUncertain significance
Select item 2336886	NM_007374.3(SIX6):c.314G>C (p.Arg105Thr)	C14orf39, SIX6 (R105T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301864	NM_007374.3(SIX6):c.710T>C (p.Ile237Thr)	C14orf39, SIX6 (I237T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254619	NM_007374.3(SIX6):c.443T>G (p.Leu148Arg)	C14orf39, SIX6 (L148R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2202066	NM_007374.3(SIX6):c.727G>A (p.Glu243Lys)	C14orf39, SIX6 (E243K)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2191121	NM_007374.3(SIX6):c.652G>A (p.Val218Ile)	C14orf39, SIX6 (V218I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2190882	NM_007374.3(SIX6):c.591G>C (p.Leu197=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2178909	NM_007374.3(SIX6):c.65A>T (p.Glu22Val)	C14orf39, SIX6 (E22V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2171353	NM_007374.3(SIX6):c.91G>C (p.Gly31Arg)	C14orf39, SIX6 (G31R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2170602	NM_007374.3(SIX6):c.572+13A>G	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2155056	NM_007374.3(SIX6):c.369C>T (p.Arg123=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2154092	NM_007374.3(SIX6):c.435G>A (p.Glu145=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2143349	NM_007374.3(SIX6):c.135G>C (p.Glu45Asp)	C14orf39, SIX6 (E45D)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2142265	NM_007374.3(SIX6):c.185T>G (p.Phe62Cys)	C14orf39, SIX6 (F62C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2140163	NM_007374.3(SIX6):c.730T>C (p.Cys244Arg)	C14orf39, SIX6 (C244R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2119810	NM_007374.3(SIX6):c.145A>G (p.Lys49Glu)	C14orf39, SIX6 (K49E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2117133	NM_007374.3(SIX6):c.257_261del (p.Lys86fs)	C14orf39, SIX6 (K86fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 2111909	NM_007374.3(SIX6):c.627C>T (p.Gly209=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2097395	NM_007374.3(SIX6):c.12G>C (p.Leu4=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2087606	NM_007374.3(SIX6):c.636G>A (p.Thr212=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2085476	NM_007374.3(SIX6):c.121C>T (p.Pro41Ser)	C14orf39, SIX6 (P41S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2080389	NM_007374.3(SIX6):c.503C>T (p.Thr168Ile)	C14orf39, SIX6 (T168I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2080301	NM_007374.3(SIX6):c.731G>A (p.Cys244Tyr)	C14orf39, SIX6 (C244Y)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2073523	NM_007374.3(SIX6):c.616C>G (p.Arg206Gly)	C14orf39, SIX6 (R206G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2046768	NM_007374.3(SIX6):c.216T>A (p.His72Gln)	C14orf39, SIX6 (H72Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2038664	NM_007374.3(SIX6):c.691G>A (p.Ala231Thr)	C14orf39, SIX6 (A231T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2038007	NM_007374.3(SIX6):c.407A>C (p.Lys136Thr)	C14orf39, SIX6 (K136T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2007300	NM_007374.3(SIX6):c.521A>G (p.Asn174Ser)	C14orf39, SIX6 (N174S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2006087	NM_007374.3(SIX6):c.308G>T (p.Arg103Leu)	C14orf39, SIX6 (R103L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1999382	NM_007374.3(SIX6):c.476G>A (p.Arg159His)	C14orf39, SIX6 (R159H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1984992	NM_007374.3(SIX6):c.654C>T (p.Val218=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1984759	NM_007374.3(SIX6):c.515T>C (p.Val172Ala)	C14orf39, SIX6 (V172A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1979496	NM_007374.3(SIX6):c.340C>T (p.Arg114Ter)	C14orf39, SIX6 (R114*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1978360	NM_007374.3(SIX6):c.76G>A (p.Asp26Asn)	C14orf39, SIX6 (D26N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1978086	NM_007374.3(SIX6):c.613del (p.Leu205fs)	C14orf39, SIX6 (L205fs)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1962049	NM_007374.3(SIX6):c.608G>A (p.Arg203Gln)	C14orf39, SIX6 (R203Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1956412	NM_007374.3(SIX6):c.624G>A (p.Glu208=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1949417	NM_007374.3(SIX6):c.376T>C (p.Trp126Arg)	C14orf39, SIX6 (W126R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1946152	NM_007374.3(SIX6):c.732C>A (p.Cys244Ter)	C14orf39, SIX6 (C244*)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 1923574	NM_007374.3(SIX6):c.265G>A (p.Ala89Thr)	C14orf39, SIX6 (A89T)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1917425	NM_007374.3(SIX6):c.621G>A (p.Ala207=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1915101	NM_007374.3(SIX6):c.652G>T (p.Val218Phe)	C14orf39, SIX6 (V218F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1909747	NM_007374.3(SIX6):c.267G>A (p.Ala89=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1807640	GRCh37/hg19 14q22.3-23.2(chr14:57804997-63590203)x1	ACTR10, ARID4A +32 more	Copy number loss	not provided	GLikely pathogenic
Select item 1707441	GRCh37/hg19 14q13.3-32.33(chr14:37671058-106985955)x2	AREL1, ARF6 +447 more	Copy number gain	See cases	GPathogenic
Select item 1690892	NM_007374.3(SIX6):c.380del (p.Asp127fs)	C14orf39, SIX6 (D127fs)	Deletion (frameshift variant)	See cases	GLikely pathogenic
Select item 1653641	NM_007374.3(SIX6):c.243G>A (p.Lys81=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1648580	NM_007374.3(SIX6):c.216T>C (p.His72=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1648095	NM_007374.3(SIX6):c.123T>C (p.Pro41=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1612614	NM_007374.3(SIX6):c.573-10T>C	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1581643	NM_007374.3(SIX6):c.162A>C (p.Leu54=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1540993	NM_007374.3(SIX6):c.171A>G (p.Arg57=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1518516	NM_007374.3(SIX6):c.10C>A (p.Leu4Met)	C14orf39, SIX6 (L4M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1509007	NM_007374.3(SIX6):c.725_726delinsTT (p.Ser242Ile)	C14orf39, SIX6 (S242I)	Indel (missense variant)	not provided	GUncertain significance
Select item 1495929	NM_007374.3(SIX6):c.446A>G (p.Gln149Arg)	C14orf39, SIX6 (Q149R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1492575	NM_007374.3(SIX6):c.473A>C (p.Lys158Thr)	C14orf39, SIX6 (K158T)	Single nucleotide variant (missense variant)	not provided	GConflicting classifications of pathogenicity
Select item 1474246	NM_007374.3(SIX6):c.410A>C (p.Glu137Ala)	C14orf39, SIX6 (E137A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1425830	NM_007374.3(SIX6):c.579G>C (p.Gln193His)	C14orf39, SIX6 (Q193H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1341150	GRCh37/hg19 14q23.1(chr14:60958879-61211351)x3	MNAT1, SIX1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 1296515	NM_007374.3(SIX6):c.573-184G>A	C14orf39, SIX6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1162192	GRCh37/hg19 14q22.2-24.3(chr14:54654001-75828024)x3	ISCA2, TMEM30B +158 more	Copy number gain	14q22.2q24.3 duplication	GLikely pathogenic
Select item 999901	NC_000014.8:g.(?_60976117)_(61191013_?)dup	SIX1, SIX4 +1 more	Duplication	Autosomal dominant nonsyndromic hearing loss 23 +1 more	GUncertain significance
Select item 980497	GRCh37/hg19 14q23.1(chr14:60841069-61002469)x3	C14orf39, SIX6	Copy number gain	not provided	GUncertain significance
Select item 980496	GRCh37/hg19 14q23.1(chr14:60958879-61194753)x3	SIX1, SIX6 +1 more	Copy number gain	not provided	GUncertain significance
Select item 883966	NM_007374.3(SIX6):c.725G>T (p.Ser242Ile)	C14orf39, SIX6 (S242I)	Single nucleotide variant (missense variant)	Anophthalmia-microphthalmia syndrome	GUncertain significance
Select item 883965	NM_007374.3(SIX6):c.714G>T (p.Thr238=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	Anophthalmia-microphthalmia syndrome	GUncertain significance
Select item 883964	NM_007374.3(SIX6):c.635C>T (p.Thr212Met)	C14orf39, SIX6 (T212M)	Single nucleotide variant (missense variant)	Anophthalmia-microphthalmia syndrome +1 more	GUncertain significance
Select item 883182	NM_007374.3(SIX6):c.389A>G (p.Gln130Arg)	C14orf39, SIX6 (Q130R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 882087	NM_007374.3(SIX6):c.*462A>G	C14orf39, SIX6	Single nucleotide variant (3 prime UTR variant)	Anophthalmia-microphthalmia syndrome	GUncertain significance
Select item 882020	NM_007374.3(SIX6):c.21G>A (p.Leu7=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 882019	NM_007374.3(SIX6):c.18C>A (p.Ile6=)	C14orf39, SIX6	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 882018	NM_007374.3(SIX6):c.-64C>T	C14orf39, SIX6	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GLikely benign
Select item 882017	NM_007374.3(SIX6):c.-147T>C	C14orf39, SIX6	Single nucleotide variant (5 prime UTR variant)	not provided +1 more	GLikely benign
Select item 880675	NM_007374.3(SIX6):c.*432G>A	C14orf39, SIX6	Single nucleotide variant (3 prime UTR variant)	Anophthalmia-microphthalmia syndrome	GUncertain significance
Select item 880674	NM_007374.3(SIX6):c.*124C>A	C14orf39, SIX6	Single nucleotide variant (3 prime UTR variant)	Anophthalmia-microphthalmia syndrome	GUncertain significance

<< First< Prev

Page of 2