ClinVar for Gene (Select 576) - ClinVar - NCBI

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

Links from Gene

Items: 1 to 100 of 284

<< First< Prev

Page of 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3270693	NM_001364857.2(ADGRB2):c.3011A>G (p.His1004Arg)	ADGRB2 (H1004R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270684	NM_001364857.2(ADGRB2):c.2553G>C (p.Gln851His)	ADGRB2 (Q851H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270675	NM_001364857.2(ADGRB2):c.345G>T (p.Glu115Asp)	ADGRB2 (E115D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270665	NM_001364857.2(ADGRB2):c.407C>T (p.Ala136Val)	ADGRB2 (A136V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270655	NM_001364857.2(ADGRB2):c.406G>A (p.Ala136Thr)	ADGRB2 (A136T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270645	NM_001364857.2(ADGRB2):c.1096G>A (p.Val366Met)	ADGRB2 (V366M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270635	NM_001364857.2(ADGRB2):c.1408G>A (p.Glu470Lys)	ADGRB2 (E470K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270623	NM_001364857.2(ADGRB2):c.1676C>T (p.Pro559Leu)	ADGRB2 (P559L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270614	NM_001364857.2(ADGRB2):c.4495C>T (p.Arg1499Cys)	ADGRB2 (R1465C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270604	NM_001364857.2(ADGRB2):c.137G>A (p.Gly46Asp)	ADGRB2 (G46D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270594	NM_001364857.2(ADGRB2):c.3115C>A (p.Leu1039Ile)	ADGRB2 (L1039I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270584	NM_001364857.2(ADGRB2):c.1289C>T (p.Pro430Leu)	ADGRB2 (P430L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270573	NM_001364857.2(ADGRB2):c.859C>G (p.Pro287Ala)	ADGRB2 (P287A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3270562	NM_001364857.2(ADGRB2):c.618G>T (p.Glu206Asp)	ADGRB2 (E206D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3252064	NM_001364857.2(ADGRB2):c.4150C>T (p.Arg1384Ter)	ADGRB2 (R1351* +1 more)	Single nucleotide variant (nonsense)	Hereditary spastic paraplegia	GUncertain significance
Select item 3084188	NM_001364857.2(ADGRB2):c.848C>T (p.Pro283Leu)	ADGRB2 (P283L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084184	NM_001364857.2(ADGRB2):c.562A>G (p.Ile188Val)	ADGRB2 (I188V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084177	NM_001364857.2(ADGRB2):c.521C>T (p.Ala174Val)	ADGRB2 (A174V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084175	NM_001364857.2(ADGRB2):c.4669C>G (p.Pro1557Ala)	ADGRB2 (P1556A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084168	NM_001364857.2(ADGRB2):c.4490G>A (p.Arg1497His)	ADGRB2 (R1496H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084160	NM_001364857.2(ADGRB2):c.4288C>T (p.Pro1430Ser)	ADGRB2 (P1397S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084156	NM_001364857.2(ADGRB2):c.3859G>A (p.Val1287Met)	ADGRB2 (V1254M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084147	NM_001364857.2(ADGRB2):c.3514G>A (p.Val1172Ile)	ADGRB2 (V1172I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084114	NM_001364857.2(ADGRB2):c.3280A>G (p.Ile1094Val)	ADGRB2 (I1094V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084101	NM_001364857.2(ADGRB2):c.2983G>A (p.Val995Met)	ADGRB2 (V995M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084090	NM_001364857.2(ADGRB2):c.2595C>G (p.Ile865Met)	ADGRB2 (I865M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084058	NM_001364857.2(ADGRB2):c.2119G>A (p.Asp707Asn)	ADGRB2 (D707N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084055	NM_001364857.2(ADGRB2):c.2024C>T (p.Ala675Val)	ADGRB2 (A675V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084047	NM_001364857.2(ADGRB2):c.1888A>G (p.Thr630Ala)	ADGRB2 (T630A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084039	NM_001364857.2(ADGRB2):c.1369A>T (p.Thr457Ser)	ADGRB2 (T457S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084022	NM_001364857.2(ADGRB2):c.1180C>T (p.Pro394Ser)	ADGRB2 (P394S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084016	NM_001364857.2(ADGRB2):c.1108T>G (p.Trp370Gly)	ADGRB2 (W370G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3084007	NM_001364857.2(ADGRB2):c.1019C>G (p.Pro340Arg)	ADGRB2 (P340R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3017211	NM_001364857.2(ADGRB2):c.2087G>A (p.Arg696His)	ADGRB2 (R696H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3016061	NM_001364857.2(ADGRB2):c.4067G>A (p.Arg1356Gln)	ADGRB2 (R1323Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3015695	NM_001364857.2(ADGRB2):c.4679G>A (p.Arg1560Gln)	ADGRB2 (R1559Q +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3011101	NM_001364857.2(ADGRB2):c.1990-20A>G	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3006446	NM_001364857.2(ADGRB2):c.904C>A (p.Leu302Ile)	ADGRB2 (L302I)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3003495	NM_001364857.2(ADGRB2):c.3476T>C (p.Val1159Ala)	ADGRB2 (V1126A +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2994538	NM_001364857.2(ADGRB2):c.637G>A (p.Gly213Ser)	ADGRB2 (G213S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2988929	NM_001364857.2(ADGRB2):c.93C>T (p.Thr31=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2984237	NM_001364857.2(ADGRB2):c.4281G>A (p.Pro1427=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2982967	NM_001364857.2(ADGRB2):c.267G>A (p.Val89=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance
Select item 2981641	NM_001364857.2(ADGRB2):c.4515+16G>A	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2981122	NM_001364857.2(ADGRB2):c.707C>G (p.Thr236Ser)	ADGRB2 (T236S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2975342	NM_001364857.2(ADGRB2):c.958G>A (p.Val320Met)	ADGRB2 (V320M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2974096	NM_001364857.2(ADGRB2):c.1449G>A (p.Ala483=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2973166	NM_001364857.2(ADGRB2):c.3353+6G>A	ADGRB2	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 2969716	NM_001364857.2(ADGRB2):c.342C>T (p.Pro114=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2968603	NM_001364857.2(ADGRB2):c.3088C>T (p.Arg1030Cys)	ADGRB2 (R1030C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2961833	NM_001364857.2(ADGRB2):c.1038C>T (p.Ser346=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2960619	NM_001364857.2(ADGRB2):c.417G>A (p.Leu139=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2958233	NM_001364857.2(ADGRB2):c.3353+18G>C	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2920184	NM_001364857.2(ADGRB2):c.472G>A (p.Val158Met)	ADGRB2 (V158M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2911586	NM_001364857.2(ADGRB2):c.4232C>T (p.Ala1411Val)	ADGRB2 (A1378V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2904759	NM_001364857.2(ADGRB2):c.2982C>T (p.Gly994=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2900782	NM_001364857.2(ADGRB2):c.4563C>T (p.Ser1521=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2897027	NM_001364857.2(ADGRB2):c.357C>T (p.Ala119=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2896822	NM_001364857.2(ADGRB2):c.4416+10A>G	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2895412	NM_001364857.2(ADGRB2):c.1341C>T (p.Ser447=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2894467	NM_001364857.2(ADGRB2):c.2603G>C (p.Gly868Ala)	ADGRB2 (G868A)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2887982	NM_001364857.2(ADGRB2):c.4735G>A (p.Gly1579Ser)	ADGRB2 (G1545S +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2886568	NM_001364857.2(ADGRB2):c.351G>A (p.Ala117=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2886162	NM_001364857.2(ADGRB2):c.1060C>T (p.Pro354Ser)	ADGRB2 (P354S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2885649	NM_001364857.2(ADGRB2):c.1374T>C (p.Gly458=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2885190	NM_001364857.2(ADGRB2):c.3025T>G (p.Ser1009Ala)	ADGRB2 (S1009A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2880798	NM_001364857.2(ADGRB2):c.1020C>A (p.Pro340=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2809721	NM_001364857.2(ADGRB2):c.677C>A (p.Pro226His)	ADGRB2 (P226H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2798738	NM_001364857.2(ADGRB2):c.1200C>T (p.Ala400=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2793167	NM_001364857.2(ADGRB2):c.656C>T (p.Ala219Val)	ADGRB2 (A219V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2790835	NM_001364857.2(ADGRB2):c.846G>A (p.Glu282=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2786067	NM_001364857.2(ADGRB2):c.1115C>T (p.Ser372Phe)	ADGRB2 (S372F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2785200	NM_001364857.2(ADGRB2):c.1381A>G (p.Thr461Ala)	ADGRB2 (T461A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2778631	NM_001364857.2(ADGRB2):c.2168-15C>G	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2777662	NM_001364857.2(ADGRB2):c.1974G>A (p.Ser658=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2772977	NM_001364857.2(ADGRB2):c.2114T>C (p.Val705Ala)	ADGRB2 (V705A)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2764617	NM_001364857.2(ADGRB2):c.839-17C>T	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2754390	NM_001364857.2(ADGRB2):c.3353+10G>A	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2750965	NM_001364857.2(ADGRB2):c.1688-15C>T	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2745616	NM_001364857.2(ADGRB2):c.2144C>T (p.Ser715Phe)	ADGRB2 (S715F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2738453	NM_001364857.2(ADGRB2):c.188C>T (p.Ser63Leu)	ADGRB2 (S63L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2724441	NM_001364857.2(ADGRB2):c.509C>T (p.Pro170Leu)	ADGRB2 (P170L)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2718746	NM_001364857.2(ADGRB2):c.972G>A (p.Thr324=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2716649	NM_001364857.2(ADGRB2):c.1346C>T (p.Ala449Val)	ADGRB2 (A449V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2716623	NM_001364857.2(ADGRB2):c.2760G>A (p.Pro920=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2716212	NM_001364857.2(ADGRB2):c.3817C>T (p.Arg1273Cys)	ADGRB2 (R1240C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2712978	NM_001364857.2(ADGRB2):c.4134G>A (p.Pro1378=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2711262	NM_001364857.2(ADGRB2):c.3314G>A (p.Arg1105His)	ADGRB2 (R1105H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2710469	NM_001364857.2(ADGRB2):c.363G>A (p.Ala121=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2701212	NM_001364857.2(ADGRB2):c.2334G>A (p.Gly778=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2696410	NM_001364857.2(ADGRB2):c.1989+17A>G	ADGRB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2695672	NM_001364857.2(ADGRB2):c.3789C>A (p.Asn1263Lys)	ADGRB2 (N1230K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	A2ML1-AS2, A3GALT2 +2151 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 2638605	NM_001364857.2(ADGRB2):c.4516A>C (p.Arg1506=)	ADGRB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2611263	NM_001364857.2(ADGRB2):c.3328G>A (p.Asp1110Asn)	ADGRB2 (D1110N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605151	NM_001364857.2(ADGRB2):c.1198G>A (p.Ala400Thr)	ADGRB2 (A400T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597688	NM_001364857.2(ADGRB2):c.343G>A (p.Glu115Lys)	ADGRB2 (E115K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588189	NM_001364857.2(ADGRB2):c.4541C>T (p.Ser1514Leu)	ADGRB2 (S1480L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2544253	NM_001364857.2(ADGRB2):c.1183C>A (p.Gln395Lys)	ADGRB2 (Q395K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540722	NM_001364857.2(ADGRB2):c.1121G>A (p.Ser374Asn)	ADGRB2 (S374N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

<< First< Prev

Page of 3