"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "ADAMTS1 - ClinVar - NCBI

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

Search results

Items: 1 to 100 of 691

<< First< Prev

Page of 7

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2719916	NM_030957.4(ADAMTS10):c.3306C>A (p.Gly1102=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1573212	NM_030957.4(ADAMTS10):c.3306C>T (p.Gly1102=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 518307	NM_030957.4(ADAMTS10):c.3303T>G (p.His1101Gln)	ADAMTS10 (H1101Q +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1550112	NM_030957.4(ADAMTS10):c.3300C>T (p.Cys1100=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2017635	NM_030957.4(ADAMTS10):c.3282del (p.Met1095fs)	ADAMTS10 (M582fs +1 more)	Deletion (frameshift variant)	not provided	GUncertain significance
Select item 1392003	NM_030957.4(ADAMTS10):c.3277C>A (p.Arg1093Ser)	ADAMTS10 (R580S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2981194	NM_030957.4(ADAMTS10):c.3270C>G (p.Ala1090=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2140209	NM_030957.4(ADAMTS10):c.3264C>A (p.Ser1088Arg)	ADAMTS10 (S1088R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 595050	NM_030957.4(ADAMTS10):c.3262A>G (p.Ser1088Gly)	ADAMTS10 (S1088G +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1 +2 more	GUncertain significance
Select item 1408887	NM_030957.4(ADAMTS10):c.3244C>G (p.Leu1082Val)	ADAMTS10 (L1082V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2846639	NM_030957.4(ADAMTS10):c.3234C>T (p.Cys1078=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1393213	NM_030957.4(ADAMTS10):c.3221A>G (p.Lys1074Arg)	ADAMTS10 (K1074R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 799379	NM_030957.4(ADAMTS10):c.3216G>C (p.Val1072=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2728840	NM_030957.4(ADAMTS10):c.3203-6_3203-5del	ADAMTS10	Deletion (intron variant)	not provided	GLikely benign
Select item 1989651	NM_030957.4(ADAMTS10):c.3203-5C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1085700	NM_030957.4(ADAMTS10):c.3203-7C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1993721	NM_030957.4(ADAMTS10):c.3203-8C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2135540	NM_030957.4(ADAMTS10):c.3203-10G>C	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2960327	NM_030957.4(ADAMTS10):c.3203-11C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967757	NM_030957.4(ADAMTS10):c.3203-12C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1615202	NM_030957.4(ADAMTS10):c.3203-13C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3000201	NM_030957.4(ADAMTS10):c.3203-15C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1958694	NM_030957.4(ADAMTS10):c.3203-18_3203-15del	ADAMTS10	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2986282	NM_030957.4(ADAMTS10):c.3203-19C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1395371	NM_030957.4(ADAMTS10):c.3202+9del	ADAMTS10	Deletion (intron variant)	not provided	GLikely benign
Select item 2798604	NM_030957.4(ADAMTS10):c.3195C>A (p.Gly1065=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 81472	NM_030957.4(ADAMTS10):c.3193G>A (p.Gly1065Ser)	ADAMTS10 (G1065S +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome +2 more	GBenign/Likely benign
Select item 1982056	NM_030957.4(ADAMTS10):c.3182C>A (p.Thr1061Asn)	ADAMTS10 (T1061N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1347511	NM_030957.4(ADAMTS10):c.3177C>A (p.Ser1059Arg)	ADAMTS10 (S546R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2111554	NM_030957.4(ADAMTS10):c.3172G>C (p.Asp1058His)	ADAMTS10 (D1058H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2881870	NM_030957.4(ADAMTS10):c.3165C>T (p.Ala1055=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2862729	NM_030957.4(ADAMTS10):c.3154C>T (p.Gln1052Ter)	ADAMTS10 (Q539* +1 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 3011231	NM_030957.4(ADAMTS10):c.3153G>A (p.Gln1051=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2117460	NM_030957.4(ADAMTS10):c.3150G>A (p.Thr1050=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2045738	NM_030957.4(ADAMTS10):c.3149C>T (p.Thr1050Met)	ADAMTS10 (T1050M +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1379013	NM_030957.4(ADAMTS10):c.3149C>G (p.Thr1050Arg)	ADAMTS10 (T1050R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1566439	NM_030957.4(ADAMTS10):c.3141G>T (p.Pro1047=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1908290	NM_030957.4(ADAMTS10):c.3138G>A (p.Arg1046=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2888447	NM_030957.4(ADAMTS10):c.3133C>T (p.Leu1045=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1399921	NM_030957.4(ADAMTS10):c.3123C>T (p.Cys1041=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1973907	NM_030957.4(ADAMTS10):c.3120G>A (p.Glu1040=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1904335	NM_030957.4(ADAMTS10):c.3116A>C (p.His1039Pro)	ADAMTS10 (H1039P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2963350	NM_030957.4(ADAMTS10):c.3114G>T (p.Ser1038=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1930089	NM_030957.4(ADAMTS10):c.3108G>C (p.Gln1036His)	ADAMTS10 (Q1036H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2693248	NM_030957.4(ADAMTS10):c.3105C>A (p.Gly1035=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 330579	NM_030957.4(ADAMTS10):c.3102G>A (p.Thr1034=)	ADAMTS10	Single nucleotide variant (synonymous variant)	Weill-Marchesani syndrome +1 more	GBenign/Likely benign
Select item 1426981	NM_030957.4(ADAMTS10):c.3097C>T (p.His1033Tyr)	ADAMTS10 (H1033Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1920270	NM_030957.4(ADAMTS10):c.3092C>A (p.Thr1031Asn)	ADAMTS10 (T1031N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1720491	NM_030957.4(ADAMTS10):c.3085C>A (p.Arg1029Ser)	ADAMTS10 (R1029S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1975198	NM_030957.4(ADAMTS10):c.3084G>A (p.Val1028=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1115032	NM_030957.4(ADAMTS10):c.3081G>A (p.Ser1027=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2090289	NM_030957.4(ADAMTS10):c.3079T>C (p.Ser1027Pro)	ADAMTS10 (S1027P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2775528	NM_030957.4(ADAMTS10):c.3066G>A (p.Gly1022=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1632559	NM_030957.4(ADAMTS10):c.3066G>C (p.Gly1022=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2724083	NM_030957.4(ADAMTS10):c.3060C>T (p.Gly1020=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2020426	NM_030957.4(ADAMTS10):c.3060C>G (p.Gly1020=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2707739	NM_030957.4(ADAMTS10):c.3051A>G (p.Ala1017=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1535520	NM_030957.4(ADAMTS10):c.3045C>T (p.Cys1015=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976341	NM_030957.4(ADAMTS10):c.3043-5_3043-4insCCCCCTT	ADAMTS10	Insertion (intron variant)	not provided	GLikely benign
Select item 3013222	NM_030957.4(ADAMTS10):c.3043-5C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1572817	NM_030957.4(ADAMTS10):c.3043-5C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 330580	NM_030957.3(ADAMTS10):c.3043-12_3043-6dup	ADAMTS10	Duplication (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 2896332	NM_030957.4(ADAMTS10):c.3043-12_3043-7dup	ADAMTS10	Duplication (intron variant)	not provided	GLikely benign
Select item 330581	NM_030957.4(ADAMTS10):c.3043-8C>T	ADAMTS10	Single nucleotide variant (intron variant)	Weill-Marchesani syndrome +1 more	GConflicting classifications of pathogenicity
Select item 1501801	NM_030957.4(ADAMTS10):c.3043-10C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1651083	NM_030957.4(ADAMTS10):c.3042+17del	ADAMTS10	Deletion (intron variant)	not provided	GBenign
Select item 1533178	NM_030957.4(ADAMTS10):c.3042+16C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3012426	NM_030957.4(ADAMTS10):c.3024G>A (p.Val1008=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1448249	NM_030957.4(ADAMTS10):c.3017G>A (p.Arg1006His)	ADAMTS10 (R1006H +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1018281	NM_030957.4(ADAMTS10):c.3011C>T (p.Pro1004Leu)	ADAMTS10 (P1004L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1618589	NM_030957.4(ADAMTS10):c.3006C>T (p.Cys1002=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2996355	NM_030957.4(ADAMTS10):c.2983A>G (p.Met995Val)	ADAMTS10 (M995V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2967000	NM_030957.4(ADAMTS10):c.2983A>T (p.Met995Leu)	ADAMTS10 (M482L +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1533448	NM_030957.4(ADAMTS10):c.2982C>G (p.Thr994=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1523731	NM_030957.4(ADAMTS10):c.2980A>G (p.Thr994Ala)	ADAMTS10 (T481A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2080241	NM_030957.4(ADAMTS10):c.2976G>T (p.Pro992=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2173201	NM_030957.4(ADAMTS10):c.2961C>G (p.Pro987=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1591042	NM_030957.4(ADAMTS10):c.2961C>T (p.Pro987=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1933651	NM_030957.4(ADAMTS10):c.2948C>A (p.Ala983Glu)	ADAMTS10 (A470E +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1549670	NM_030957.4(ADAMTS10):c.2943C>T (p.Pro981=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1425850	NM_030957.4(ADAMTS10):c.2938C>G (p.Leu980Val)	ADAMTS10 (L467V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2970763	NM_030957.4(ADAMTS10):c.2937G>A (p.Thr979=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1991407	NM_030957.4(ADAMTS10):c.2925C>T (p.Asp975=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1932478	NM_030957.4(ADAMTS10):c.2918G>C (p.Ser973Thr)	ADAMTS10 (S973T +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1990093	NM_030957.4(ADAMTS10):c.2908C>T (p.Leu970Phe)	ADAMTS10 (L457F +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1902261	NM_030957.4(ADAMTS10):c.2895C>A (p.Arg965=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2177696	NM_030957.4(ADAMTS10):c.2886G>C (p.Pro962=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3001048	NM_030957.4(ADAMTS10):c.2880C>T (p.Cys960=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1487054	NM_030957.4(ADAMTS10):c.2875A>G (p.Ser959Gly)	ADAMTS10 (S446G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2855195	NM_030957.4(ADAMTS10):c.2871C>A (p.Thr957=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1715982	NM_030957.4(ADAMTS10):c.2866T>G (p.Cys956Gly)	ADAMTS10 (C443G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2420589	NM_030957.4(ADAMTS10):c.2866-13C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2993784	NM_030957.4(ADAMTS10):c.2866-16C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2110736	NM_030957.4(ADAMTS10):c.2865+20C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1951301	NM_030957.4(ADAMTS10):c.2865+20C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 894780	NM_030957.4(ADAMTS10):c.2865+11C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1554184	NM_030957.4(ADAMTS10):c.2865+9C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1964478	NM_030957.4(ADAMTS10):c.2847G>T (p.Ala949=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 730428	NM_030957.4(ADAMTS10):c.2845G>A (p.Ala949Thr)	ADAMTS10 (A949T +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1 +1 more	GConflicting classifications of pathogenicity
Select item 1373978	NM_030957.4(ADAMTS10):c.2838G>A (p.Pro946=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

<< First< Prev

Page of 7