ClinVar for Gene (Select 81794) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3146691	NM_030957.4(ADAMTS10):c.685C>A (p.Pro229Thr)	ADAMTS10 (P229T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146650	NM_030957.4(ADAMTS10):c.2800C>A (p.Pro934Thr)	ADAMTS10 (P421T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146641	NM_030957.4(ADAMTS10):c.2581G>A (p.Val861Ile)	ADAMTS10 (V348I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146639	NM_030957.4(ADAMTS10):c.2336G>A (p.Arg779Gln)	ADAMTS10 (R779Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146628	NM_030957.4(ADAMTS10):c.2194G>A (p.Val732Ile)	ADAMTS10 (V732I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146624	NM_030957.4(ADAMTS10):c.2072G>A (p.Arg691Gln)	ADAMTS10 (R691Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3146588	NM_030957.4(ADAMTS10):c.1394C>T (p.Pro465Leu)	ADAMTS10 (P465L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3068001	NM_030957.4(ADAMTS10):c.2888G>A (p.Gly963Asp)	ADAMTS10 (G450D +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1	GUncertain significance
Select item 3065634	NM_030957.4(ADAMTS10):c.2707G>C (p.Gly903Arg)	ADAMTS10 (G390R +1 more)	Single nucleotide variant (missense variant)	Weill-Marchesani syndrome 1	GLikely benign
Select item 3023108	NM_030957.4(ADAMTS10):c.89-9C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021882	NM_030957.4(ADAMTS10):c.1248A>G (p.Pro416=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3017026	NM_030957.4(ADAMTS10):c.1901-18C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3016876	NM_030957.4(ADAMTS10):c.2530+12G>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3016667	NM_030957.4(ADAMTS10):c.2088A>G (p.Arg696=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3015266	NM_030957.4(ADAMTS10):c.2631C>A (p.Arg877=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3013844	NM_030957.4(ADAMTS10):c.2793G>C (p.Pro931=)	ADAMTS10	Single nucleotide variant (synonymous 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 3012426	NM_030957.4(ADAMTS10):c.3024G>A (p.Val1008=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3011231	NM_030957.4(ADAMTS10):c.3153G>A (p.Gln1051=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3010974	NM_030957.4(ADAMTS10):c.447C>T (p.Ile149=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3008356	NM_030957.4(ADAMTS10):c.1734-8C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3004493	NM_030957.4(ADAMTS10):c.1900+18A>G	ADAMTS10	Single nucleotide variant (intron 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 3000201	NM_030957.4(ADAMTS10):c.3203-15C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2999262	NM_030957.4(ADAMTS10):c.1733+15C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2997699	NM_030957.4(ADAMTS10):c.1623G>A (p.Ser541=)	ADAMTS10 (R32H)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2996906	NM_030957.4(ADAMTS10):c.1074C>T (p.Cys358=)	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 2996153	NM_030957.4(ADAMTS10):c.1587+11G>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995253	NM_030957.4(ADAMTS10):c.1632G>A (p.Glu544=)	ADAMTS10 (R35K)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2994359	NM_030957.4(ADAMTS10):c.1904G>T (p.Gly635Val)	ADAMTS10 (G635V)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2993811	NM_030957.4(ADAMTS10):c.435+10G>A	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 2992302	NM_030957.4(ADAMTS10):c.1371C>T (p.Pro457=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2991508	NM_030957.4(ADAMTS10):c.2404-15G>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2989343	NM_030957.4(ADAMTS10):c.657C>A (p.Pro219=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2989255	NM_030957.4(ADAMTS10):c.2530+11G>C	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2988271	NM_030957.4(ADAMTS10):c.1548C>A (p.Ala516=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2987728	NM_030957.4(ADAMTS10):c.1584G>A (p.Lys528=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2987544	NM_030957.4(ADAMTS10):c.6T>C (p.Ala2=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2986775	NM_030957.4(ADAMTS10):c.1905C>T (p.Gly635=)	ADAMTS10	Single nucleotide variant (synonymous variant +1 more)	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 2984854	NM_030957.4(ADAMTS10):c.2046C>T (p.Cys682=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2983853	NM_030957.4(ADAMTS10):c.1798-16C>A	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983423	NM_030957.4(ADAMTS10):c.1588-7C>A	ADAMTS10 (P18Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2983295	NM_030957.4(ADAMTS10):c.1181T>C (p.Ile394Thr)	ADAMTS10 (I394T)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2982470	NM_030957.4(ADAMTS10):c.2619C>G (p.Pro873=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2981194	NM_030957.4(ADAMTS10):c.3270C>G (p.Ala1090=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2980466	NM_030957.4(ADAMTS10):c.2531-14del	ADAMTS10	Deletion (intron variant)	not provided	GLikely benign
Select item 2980251	NM_030957.4(ADAMTS10):c.1588-7C>T	ADAMTS10 (P18L)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2978829	NM_030957.4(ADAMTS10):c.360C>T (p.Pro120=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2978406	NM_030957.4(ADAMTS10):c.963C>T (p.Ile321=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2977335	NM_030957.4(ADAMTS10):c.2035-17A>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2977045	NM_030957.4(ADAMTS10):c.882C>T (p.Leu294=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2976956	NM_030957.4(ADAMTS10):c.1338-18G>A	ADAMTS10	Single nucleotide variant (intron 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 2974893	NM_030957.4(ADAMTS10):c.1191-13C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2974832	NM_030957.4(ADAMTS10):c.123C>T (p.Ile41=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2973318	NM_030957.4(ADAMTS10):c.895-12G>C	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973165	NM_030957.4(ADAMTS10):c.2530+13G>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2970763	NM_030957.4(ADAMTS10):c.2937G>A (p.Thr979=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968870	NM_030957.4(ADAMTS10):c.194G>A (p.Arg65His)	ADAMTS10 (R65H)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2967879	NM_030957.4(ADAMTS10):c.2403+8G>A	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 2967608	NM_030957.4(ADAMTS10):c.1901-14G>C	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2967000	NM_030957.4(ADAMTS10):c.2983A>T (p.Met995Leu)	ADAMTS10 (M482L +1 more)	Single nucleotide variant (missense variant)	ADAMTS10-related condition +1 more	GUncertain significance
Select item 2965986	NM_030957.4(ADAMTS10):c.1084+13C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2963350	NM_030957.4(ADAMTS10):c.3114G>T (p.Ser1038=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2962099	NM_030957.4(ADAMTS10):c.224G>A (p.Arg75His)	ADAMTS10 (R75H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2960327	NM_030957.4(ADAMTS10):c.3203-11C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2958449	NM_030957.4(ADAMTS10):c.1293C>T (p.Phe431=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2955609	NM_030957.4(ADAMTS10):c.647C>T (p.Pro216Leu)	ADAMTS10 (P216L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2918986	NM_030957.4(ADAMTS10):c.1466A>T (p.Gln489Leu)	ADAMTS10 (Q489L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2901351	NM_030957.4(ADAMTS10):c.1371C>G (p.Pro457=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2899529	NM_030957.4(ADAMTS10):c.2061C>T (p.Gly687=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896332	NM_030957.4(ADAMTS10):c.3043-12_3043-7dup	ADAMTS10	Duplication (intron variant)	not provided	GLikely benign
Select item 2891444	NM_030957.4(ADAMTS10):c.2691C>T (p.Ser897=)	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 2885437	NM_030957.4(ADAMTS10):c.1734-5T>C	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2881870	NM_030957.4(ADAMTS10):c.3165C>T (p.Ala1055=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2878148	NM_030957.4(ADAMTS10):c.1901-11G>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2875005	NM_030957.4(ADAMTS10):c.1087C>T (p.Leu363=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2872963	NM_030957.4(ADAMTS10):c.1798-15C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2872962	NM_030957.4(ADAMTS10):c.1900+16C>G	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2869946	NM_030957.4(ADAMTS10):c.537G>A (p.Val179=)	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 2855195	NM_030957.4(ADAMTS10):c.2871C>A (p.Thr957=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2852970	NM_030957.4(ADAMTS10):c.2379G>A (p.Pro793=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2851397	NM_030957.4(ADAMTS10):c.113G>A (p.Ser38Asn)	ADAMTS10 (S38N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2851144	NM_030957.4(ADAMTS10):c.895-4C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2846639	NM_030957.4(ADAMTS10):c.3234C>T (p.Cys1078=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2839389	NM_030957.4(ADAMTS10):c.1190+8C>T	ADAMTS10	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2836399	NM_030957.4(ADAMTS10):c.1557G>C (p.Thr519=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2836036	NM_030957.4(ADAMTS10):c.213A>T (p.Thr71=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2833270	NM_030957.4(ADAMTS10):c.2409G>T (p.Leu803=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2828829	NM_030957.4(ADAMTS10):c.1374C>G (p.Pro458=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2824942	NM_030957.4(ADAMTS10):c.1731C>A (p.Pro577=)	ADAMTS10 (P68Q)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 2813386	NM_030957.4(ADAMTS10):c.632C>T (p.Thr211Ile)	ADAMTS10 (T211I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2810268	NM_030957.4(ADAMTS10):c.612G>A (p.Gly204=)	ADAMTS10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2799462	NM_030957.4(ADAMTS10):c.1588-10C>A	ADAMTS10 (P17H)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign

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