ADGRG4[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3271847	NM_153834.4(ADGRG4):c.11A>G (p.His4Arg)	ADGRG4 (H4R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3271873	NM_153834.4(ADGRG4):c.61T>C (p.Phe21Leu)	ADGRG4 (F21L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2328074	NM_153834.4(ADGRG4):c.82C>A (p.Leu28Ile)	ADGRG4 (L28I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3036705	NM_153834.4(ADGRG4):c.130A>C (p.Ser44Arg)	ADGRG4 (S44R)	Single nucleotide variant (missense variant)	ADGRG4-related disorder	GLikely benign
Select item 3086218	NM_153834.4(ADGRG4):c.140A>T (p.Asp47Val)	ADGRG4 (D47V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086288	NM_153834.4(ADGRG4):c.254G>A (p.Arg85Lys)	ADGRG4 (R85K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086328	NM_153834.4(ADGRG4):c.331C>T (p.Arg111Cys)	ADGRG4 (R111C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271943	NM_153834.4(ADGRG4):c.344C>T (p.Ala115Val)	ADGRG4 (A115V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086374	NM_153834.4(ADGRG4):c.467G>A (p.Gly156Glu)	ADGRG4 (G156E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2690849	NM_153834.4(ADGRG4):c.559C>T (p.Leu187Phe)	ADGRG4 (L187F)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 2328621	NM_153834.4(ADGRG4):c.583G>A (p.Glu195Lys)	ADGRG4 (E195K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223963	NM_153834.4(ADGRG4):c.634G>A (p.Val212Ile)	ADGRG4 (V212I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2378914	NM_153834.4(ADGRG4):c.661A>G (p.Thr221Ala)	ADGRG4 (T221A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396210	NM_153834.4(ADGRG4):c.680G>A (p.Arg227His)	ADGRG4 (R227H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050739	NM_153834.4(ADGRG4):c.686-3dup	ADGRG4	Duplication (intron variant)	ADGRG4-related disorder	GLikely benign
Select item 3051572	NM_153834.4(ADGRG4):c.758C>A (p.Ser253Tyr)	ADGRG4 (S253Y)	Single nucleotide variant (missense variant)	ADGRG4-related disorder	GLikely benign
Select item 3086486	NM_153834.4(ADGRG4):c.784A>G (p.Asn262Asp)	ADGRG4 (N262D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293729	NM_153834.4(ADGRG4):c.794A>G (p.His265Arg)	ADGRG4 (H265R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086507	NM_153834.4(ADGRG4):c.836C>G (p.Thr279Ser)	ADGRG4 (T279S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207387	NM_153834.4(ADGRG4):c.853T>A (p.Ser285Thr)	ADGRG4 (S285T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347413	NM_153834.4(ADGRG4):c.947A>T (p.Asp316Val)	ADGRG4 (D316V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611598	NM_153834.4(ADGRG4):c.998T>C (p.Ile333Thr)	ADGRG4 (I333T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271962	NM_153834.4(ADGRG4):c.1028C>G (p.Thr343Arg)	ADGRG4 (T343R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086198	NM_153834.4(ADGRG4):c.1028C>A (p.Thr343Lys)	ADGRG4 (T343K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271906	NM_153834.4(ADGRG4):c.1109C>T (p.Pro370Leu)	ADGRG4 (P370L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401449	NM_153834.4(ADGRG4):c.1184C>T (p.Ser395Leu)	ADGRG4 (S395L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086207	NM_153834.4(ADGRG4):c.1217C>A (p.Thr406Asn)	ADGRG4 (T406N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086213	NM_153834.4(ADGRG4):c.1282C>T (p.Leu428Phe)	ADGRG4 (L428F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370685	NM_153834.4(ADGRG4):c.1420A>C (p.Ile474Leu)	ADGRG4 (I474L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228609	NM_153834.4(ADGRG4):c.1495A>G (p.Lys499Glu)	ADGRG4 (K499E)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2492950	NM_153834.4(ADGRG4):c.1606T>C (p.Ser536Pro)	ADGRG4 (S536P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381518	NM_153834.4(ADGRG4):c.1666A>T (p.Thr556Ser)	ADGRG4 (T556S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086229	NM_153834.4(ADGRG4):c.1693T>C (p.Phe565Leu)	ADGRG4 (F565L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086236	NM_153834.4(ADGRG4):c.1710T>A (p.Ser570Arg)	ADGRG4 (S570R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271966	NM_153834.4(ADGRG4):c.1738A>G (p.Thr580Ala)	ADGRG4 (T580A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2257779	NM_153834.4(ADGRG4):c.1741C>T (p.Arg581Cys)	ADGRG4 (R581C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521019	NM_153834.4(ADGRG4):c.1744A>G (p.Thr582Ala)	ADGRG4 (T582A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086250	NM_153834.4(ADGRG4):c.1771G>A (p.Ala591Thr)	ADGRG4 (A591T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350648	NM_153834.4(ADGRG4):c.1813G>A (p.Gly605Arg)	ADGRG4 (G605R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271832	NM_153834.4(ADGRG4):c.1841C>T (p.Thr614Ile)	ADGRG4 (T614I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661509	NM_153834.4(ADGRG4):c.1854C>T (p.His618=)	ADGRG4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2265390	NM_153834.4(ADGRG4):c.1910G>A (p.Gly637Asp)	ADGRG4 (G637D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544254	NM_153834.4(ADGRG4):c.1948T>C (p.Ser650Pro)	ADGRG4 (S650P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544255	NM_153834.4(ADGRG4):c.1949C>T (p.Ser650Phe)	ADGRG4 (S650F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2661510	NM_153834.4(ADGRG4):c.1955A>G (p.Asn652Ser)	ADGRG4 (N652S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 1205895	NM_153834.4(ADGRG4):c.1963A>G (p.Ile655Val)	ADGRG4 (I655V)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2661511	NM_153834.4(ADGRG4):c.2022C>T (p.Leu674=)	ADGRG4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3086272	NM_153834.4(ADGRG4):c.2054C>T (p.Ala685Val)	ADGRG4 (A685V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298370	NM_153834.4(ADGRG4):c.2125C>A (p.Pro709Thr)	ADGRG4 (P709T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2609657	NM_153834.4(ADGRG4):c.2221A>G (p.Ile741Val)	ADGRG4 (I741V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474393	NM_153834.4(ADGRG4):c.2246C>A (p.Thr749Asn)	ADGRG4 (T749N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271956	NM_153834.4(ADGRG4):c.2267T>C (p.Leu756Pro)	ADGRG4 (L756P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410457	NM_153834.4(ADGRG4):c.2389C>T (p.Pro797Ser)	ADGRG4 (P797S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261498	NM_153834.4(ADGRG4):c.2392A>G (p.Asn798Asp)	ADGRG4 (N798D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333793	NM_153834.4(ADGRG4):c.2504T>C (p.Leu835Ser)	ADGRG4 (L835S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588375	NM_153834.4(ADGRG4):c.2587C>T (p.Pro863Ser)	ADGRG4 (P863S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086294	NM_153834.4(ADGRG4):c.2698A>G (p.Lys900Glu)	ADGRG4 (K900E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086297	NM_153834.4(ADGRG4):c.2791T>C (p.Phe931Leu)	ADGRG4 (F931L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086299	NM_153834.4(ADGRG4):c.2864C>A (p.Thr955Asn)	ADGRG4 (T955N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297948	NM_153834.4(ADGRG4):c.2890G>A (p.Glu964Lys)	ADGRG4 (E964K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350160	NM_153834.4(ADGRG4):c.2963C>T (p.Thr988Met)	ADGRG4 (T988M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3086308	NM_153834.4(ADGRG4):c.3023C>T (p.Pro1008Leu)	ADGRG4 (P1008L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256478	NM_153834.4(ADGRG4):c.3245G>A (p.Gly1082Glu)	ADGRG4 (G1082E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353294	NM_153834.4(ADGRG4):c.3257G>A (p.Arg1086His)	ADGRG4 (R1086H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3086321	NM_153834.4(ADGRG4):c.3304G>A (p.Ala1102Thr)	ADGRG4 (A1102T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344392	NM_153834.4(ADGRG4):c.3377C>T (p.Thr1126Ile)	ADGRG4 (T1126I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599760	NM_153834.4(ADGRG4):c.3467C>T (p.Ala1156Val)	ADGRG4 (A1156V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2305925	NM_153834.4(ADGRG4):c.3494C>T (p.Thr1165Met)	ADGRG4 (T1165M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2661512	NM_153834.4(ADGRG4):c.3495G>A (p.Thr1165=)	ADGRG4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3086344	NM_153834.4(ADGRG4):c.3573C>A (p.Phe1191Leu)	ADGRG4 (F1191L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460550	NM_153834.4(ADGRG4):c.3691A>G (p.Ile1231Val)	ADGRG4 (I1231V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3042098	NM_153834.4(ADGRG4):c.3697T>C (p.Ser1233Pro)	ADGRG4 (S1233P)	Single nucleotide variant (missense variant)	ADGRG4-related disorder	GLikely benign
Select item 2255267	NM_153834.4(ADGRG4):c.3707C>T (p.Thr1236Ile)	ADGRG4 (T1236I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2265524	NM_153834.4(ADGRG4):c.3712C>T (p.Arg1238Cys)	ADGRG4 (R1238C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386923	NM_153834.4(ADGRG4):c.3797G>T (p.Gly1266Val)	ADGRG4 (G1266V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248634	NM_153834.4(ADGRG4):c.3964A>C (p.Thr1322Pro)	ADGRG4 (T1322P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271863	NM_153834.4(ADGRG4):c.3971C>A (p.Ser1324Tyr)	ADGRG4 (S1324Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086359	NM_153834.4(ADGRG4):c.4183G>A (p.Glu1395Lys)	ADGRG4 (E1395K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2473609	NM_153834.4(ADGRG4):c.4253C>A (p.Thr1418Asn)	ADGRG4 (T1418N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3030359	NM_153834.4(ADGRG4):c.4256C>T (p.Thr1419Ile)	ADGRG4 (T1419I)	Single nucleotide variant (missense variant)	ADGRG4-related disorder	GUncertain significance
Select item 711173	NM_153834.4(ADGRG4):c.4269A>G (p.Ser1423=)	ADGRG4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2350754	NM_153834.4(ADGRG4):c.4292A>G (p.Asp1431Gly)	ADGRG4 (D1431G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239714	NM_153834.4(ADGRG4):c.4405T>C (p.Ser1469Pro)	ADGRG4 (S1469P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271963	NM_153834.4(ADGRG4):c.4457C>G (p.Thr1486Ser)	ADGRG4 (T1486S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2403645	NM_153834.4(ADGRG4):c.4477A>G (p.Asn1493Asp)	ADGRG4 (N1493D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525120	NM_153834.4(ADGRG4):c.4510A>T (p.Met1504Leu)	ADGRG4 (M1504L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1205842	NM_153834.4(ADGRG4):c.4639T>A (p.Cys1547Ser)	ADGRG4 (C1547S)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3271836	NM_153834.4(ADGRG4):c.4720C>T (p.Pro1574Ser)	ADGRG4 (P1574S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550208	NM_153834.4(ADGRG4):c.4727C>T (p.Thr1576Ile)	ADGRG4 (T1576I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271965	NM_153834.4(ADGRG4):c.4751G>T (p.Arg1584Ile)	ADGRG4 (R1584I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240550	NM_153834.4(ADGRG4):c.4751G>A (p.Arg1584Lys)	ADGRG4 (R1584K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245252	NM_153834.4(ADGRG4):c.4766C>G (p.Ser1589Cys)	ADGRG4 (S1589C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243369	NM_153834.4(ADGRG4):c.4810C>G (p.Gln1604Glu)	ADGRG4 (Q1604E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3271950	NM_153834.4(ADGRG4):c.4834C>T (p.Pro1612Ser)	ADGRG4 (P1612S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405301	NM_153834.4(ADGRG4):c.4853C>T (p.Ala1618Val)	ADGRG4 (A1618V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086388	NM_153834.4(ADGRG4):c.4928C>T (p.Thr1643Met)	ADGRG4 (T1643M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2609479	NM_153834.4(ADGRG4):c.5014G>T (p.Val1672Leu)	ADGRG4 (V1672L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486253	NM_153834.4(ADGRG4):c.5045C>T (p.Ser1682Phe)	ADGRG4 (S1682F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287800	NM_153834.4(ADGRG4):c.5158G>A (p.Gly1720Arg)	ADGRG4 (G1720R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475555	NM_153834.4(ADGRG4):c.5167A>G (p.Asn1723Asp)	ADGRG4 (N1723D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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