ClinVar for Gene (Select 545) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3364380	NM_001184.4(ATR):c.1294C>T (p.Arg432Cys)	ATR (R432C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3356520	NM_001184.4(ATR):c.4220A>G (p.Tyr1407Cys)	ATR (Y1343C +1 more)	Single nucleotide variant (missense variant)	ATR-related disorder	GUncertain significance
Select item 3352974	NM_001184.4(ATR):c.5955T>C (p.Pro1985=)	ATR	Single nucleotide variant (synonymous variant)	ATR-related disorder	GLikely benign
Select item 3343190	NM_001184.4(ATR):c.2840C>T (p.Thr947Ile)	ATR (T883I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3339072	NM_001184.4(ATR):c.6319+3A>G	ATR	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3339067	NM_001184.4(ATR):c.4152+8G>T	ATR	Single nucleotide variant (intron variant)	not specified	GUncertain significance
Select item 3337837	NM_001184.4(ATR):c.2976T>C (p.Thr992=)	ATR	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 3332367	NM_001184.4(ATR):c.3616G>A (p.Ala1206Thr)	ATR (A1142T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332357	NM_001184.4(ATR):c.5087G>C (p.Arg1696Thr)	ATR (R1696T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332349	NM_001184.4(ATR):c.4763T>A (p.Leu1588His)	ATR (L1588H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332337	NM_001184.4(ATR):c.7887T>A (p.Asp2629Glu)	ATR (D2629E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332265	NM_001184.4(ATR):c.7289C>T (p.Pro2430Leu)	ATR (P2366L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332255	NM_001184.4(ATR):c.5078G>T (p.Ser1693Ile)	ATR (S1693I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332244	NM_001184.4(ATR):c.5479A>G (p.Arg1827Gly)	ATR (R1763G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332235	NM_001184.4(ATR):c.3981A>C (p.Thr1327=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332225	NM_001184.4(ATR):c.244A>G (p.Met82Val)	ATR (M82V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332216	NM_001184.4(ATR):c.7070G>A (p.Arg2357Lys)	ATR (R2293K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332205	NM_001184.4(ATR):c.2436A>C (p.Leu812Phe)	ATR (L748F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332194	NM_001184.4(ATR):c.4288T>C (p.Cys1430Arg)	ATR (C1430R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332185	NM_001184.4(ATR):c.5105T>C (p.Leu1702Pro)	ATR (L1638P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332179	NM_001184.4(ATR):c.7102A>G (p.Ile2368Val)	ATR (I2368V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332176	NM_001184.4(ATR):c.4821C>A (p.Ser1607Arg)	ATR (S1607R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332168	NM_001184.4(ATR):c.3172A>T (p.Asn1058Tyr)	ATR (N994Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332165	NM_001184.4(ATR):c.5021G>T (p.Gly1674Val)	ATR (G1610V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332154	NM_001184.4(ATR):c.694A>T (p.Ile232Leu)	ATR (I232L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332145	NM_001184.4(ATR):c.5409A>G (p.Arg1803=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332138	NM_001184.4(ATR):c.2477G>A (p.Gly826Glu)	ATR (G826E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332127	NM_001184.4(ATR):c.5971C>T (p.Pro1991Ser)	ATR (P1927S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332117	NM_001184.4(ATR):c.3244C>G (p.Arg1082Gly)	ATR (R1018G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332106	NM_001184.4(ATR):c.2645G>A (p.Gly882Glu)	ATR (G818E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332096	NM_001184.4(ATR):c.7768A>G (p.Thr2590Ala)	ATR (T2590A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332085	NM_001184.4(ATR):c.5700C>T (p.Ile1900=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332075	NM_001184.4(ATR):c.3858G>A (p.Gln1286=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332065	NM_001184.4(ATR):c.570A>G (p.Gln190=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332055	NM_001184.4(ATR):c.4311C>G (p.Gly1437=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332048	NM_001184.4(ATR):c.7601G>A (p.Arg2534Lys)	ATR (R2534K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332042	NM_001184.4(ATR):c.6230A>G (p.Gln2077Arg)	ATR (Q2077R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332038	NM_001184.4(ATR):c.5946A>G (p.Leu1982=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332035	NM_001184.4(ATR):c.1395A>G (p.Ala465=)	ATR	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3332034	NM_001184.4(ATR):c.1184C>T (p.Pro395Leu)	ATR (P395L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332033	NM_001184.4(ATR):c.1230G>T (p.Glu410Asp)	ATR (E410D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332032	NM_001184.4(ATR):c.1408G>T (p.Ala470Ser)	ATR (A470S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3332027	NM_001184.4(ATR):c.1989C>A (p.Ser663=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3332007	NM_001184.4(ATR):c.4971C>T (p.His1657=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331989	NM_001184.4(ATR):c.7385C>T (p.Ala2462Val)	ATR (A2462V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331980	NM_001184.4(ATR):c.4840G>A (p.Val1614Ile)	ATR (V1550I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331973	NM_001184.4(ATR):c.3949A>G (p.Lys1317Glu)	ATR (K1253E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331965	NM_001184.4(ATR):c.6561T>C (p.Tyr2187=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331956	NM_001184.4(ATR):c.5302G>C (p.Asp1768His)	ATR (D1704H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331945	NM_001184.4(ATR):c.489T>A (p.Asn163Lys)	ATR (N163K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331942	NM_001184.4(ATR):c.1333C>G (p.Pro445Ala)	ATR (P445A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331936	NM_001184.4(ATR):c.5058T>A (p.Pro1686=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331934	NM_001184.4(ATR):c.3359C>G (p.Ala1120Gly)	ATR (A1056G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331930	NM_001184.4(ATR):c.384T>C (p.Cys128=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331924	NM_001184.4(ATR):c.857A>C (p.Asp286Ala)	ATR (D286A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331919	NM_001184.4(ATR):c.4698C>T (p.Thr1566=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331917	NM_001184.4(ATR):c.4654A>G (p.Ile1552Val)	ATR (I1488V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331911	NM_001184.4(ATR):c.5668A>G (p.Thr1890Ala)	ATR (T1826A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331900	NM_001184.4(ATR):c.5311A>C (p.Asn1771His)	ATR (N1707H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331891	NM_001184.4(ATR):c.1372C>G (p.Gln458Glu)	ATR (Q458E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3331881	NM_001184.4(ATR):c.3873C>A (p.Ala1291=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331871	NM_001184.4(ATR):c.2456A>T (p.Asp819Val)	ATR (D755V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331853	NM_001184.4(ATR):c.4742T>G (p.Val1581Gly)	ATR (V1517G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331845	NM_001184.4(ATR):c.4086G>T (p.Gly1362=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331836	NM_001184.4(ATR):c.4607T>C (p.Val1536Ala)	ATR (V1472A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331826	NM_001184.4(ATR):c.22C>G (p.Leu8Val)	ATR, LOC129937703 (L8V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331816	NM_001184.4(ATR):c.77A>G (p.Tyr26Cys)	ATR (Y26C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331806	NM_001184.4(ATR):c.1222A>G (p.Ile408Val)	ATR (I408V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331797	NM_001184.4(ATR):c.1395A>T (p.Ala465=)	ATR	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 3331786	NM_001184.4(ATR):c.4112T>G (p.Phe1371Cys)	ATR (F1307C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331775	NM_001184.4(ATR):c.5734A>C (p.Lys1912Gln)	ATR (K1912Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331766	NM_001184.4(ATR):c.434T>A (p.Leu145His)	ATR (L145H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331756	NM_001184.4(ATR):c.4531T>C (p.Phe1511Leu)	ATR (F1511L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331747	NM_001184.4(ATR):c.2256A>G (p.Glu752=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331736	NM_001184.4(ATR):c.4375A>C (p.Asn1459His)	ATR (N1459H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331726	NM_001184.4(ATR):c.5590A>G (p.Ile1864Val)	ATR (I1800V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331715	NM_001184.4(ATR):c.6127G>A (p.Ala2043Thr)	ATR, LOC126806830 (A1979T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331704	NM_001184.4(ATR):c.4625A>C (p.Gln1542Pro)	ATR (Q1542P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331694	NM_001184.4(ATR):c.7501A>C (p.Lys2501Gln)	ATR (K2501Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331683	NM_001184.4(ATR):c.1483G>A (p.Val495Ile)	ATR (V495I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3331675	NM_001184.4(ATR):c.111G>T (p.Leu37=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331664	NM_001184.4(ATR):c.302A>T (p.Asn101Ile)	ATR (N101I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331654	NM_001184.4(ATR):c.4194G>A (p.Met1398Ile)	ATR (M1334I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331643	NM_001184.4(ATR):c.7672C>T (p.Leu2558=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331632	NM_001184.4(ATR):c.2943T>G (p.Val981=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331621	NM_001184.4(ATR):c.1696G>T (p.Val566Leu)	ATR (V502L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331610	NM_001184.4(ATR):c.3356T>C (p.Met1119Thr)	ATR (M1119T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331591	NM_001184.4(ATR):c.3291T>C (p.Leu1097=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331582	NM_001184.4(ATR):c.7612G>T (p.Val2538Phe)	ATR (V2538F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331562	NM_001184.4(ATR):c.3671A>C (p.His1224Pro)	ATR (H1160P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331554	NM_001184.4(ATR):c.6379A>T (p.Thr2127Ser)	ATR (T2127S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331543	NM_001184.4(ATR):c.2229G>T (p.Arg743Ser)	ATR (R743S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331533	NM_001184.4(ATR):c.855T>G (p.Thr285=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331522	NM_001184.4(ATR):c.2248C>G (p.Gln750Glu)	ATR (Q686E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331513	NM_001184.4(ATR):c.1968C>T (p.Tyr656=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331502	NM_001184.4(ATR):c.7379C>T (p.Ser2460Phe)	ATR (S2396F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331481	NM_001184.4(ATR):c.1668A>T (p.Lys556Asn)	ATR (K492N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331470	NM_001184.4(ATR):c.912C>T (p.Pro304=)	ATR	Single nucleotide variant (synonymous variant)	Inborn genetic diseases	GLikely benign
Select item 3331461	NM_001184.4(ATR):c.3191T>C (p.Leu1064Pro)	ATR (L1000P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3331450	NM_001184.4(ATR):c.3005T>A (p.Leu1002His)	ATR (L1002H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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