ADGRG7[gene] - ClinVar

Search results

Items: 91

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154258	GRCh38/hg38 3q11.1-24(chr3:93800620-145695381)x3	PDIA5, PHLDB2 +1344 more	Copy number gain	See cases	GPathogenic
Select item 155192	GRCh38/hg38 3q11.1-13.11(chr3:93819623-103888749)x3	LOC112935964, LOC112935965 +171 more	Copy number gain	See cases	GLikely pathogenic
Select item 145994	GRCh38/hg38 3q11.1-13.31(chr3:93819623-116887056)x1	ABHD10, ABI3BP +431 more	Copy number loss	See cases	GPathogenic
Select item 57803	GRCh38/hg38 3q11.1-21.1(chr3:93886671-123216683)x1	TRAT1, TRMT10C +638 more	Copy number loss	See cases	GPathogenic
Select item 2579175	GRCh38/hg38 3q11.1-21.2(chr3:93979547-124774010)x1	CCDC54-AS1, LOC123002328 +682 more	Copy number loss	Chromosome 3q13.31 deletion syndrome	GPathogenic
Select item 149128	GRCh38/hg38 3q11.2-13.31(chr3:97795369-115663349)x1	ABHD10, ABI3BP +398 more	Copy number loss	See cases	GPathogenic
Select item 716103	NM_032787.3(ADGRG7):c.33G>C (p.Val11=)	ADGRG7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2350946	NM_032787.3(ADGRG7):c.64G>T (p.Gly22Cys)	ADGRG7 (G22C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272015	NM_032787.3(ADGRG7):c.145A>G (p.Thr49Ala)	ADGRG7 (T49A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272070	NM_032787.3(ADGRG7):c.150G>T (p.Glu50Asp)	ADGRG7 (E50D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272036	NM_032787.3(ADGRG7):c.242A>G (p.Glu81Gly)	ADGRG7 (E81G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086987	NM_032787.3(ADGRG7):c.269T>C (p.Phe90Ser)	ADGRG7 (F90S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312870	NM_032787.3(ADGRG7):c.316G>A (p.Gly106Ser)	ADGRG7 (G106S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272025	NM_032787.3(ADGRG7):c.317G>T (p.Gly106Val)	ADGRG7 (G106V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 156877	CM000665.1:g.100351696_100437892dup	ADGRG7, LOC129937149 +2 more	Duplication	Gestational diabetes mellitus uncontrolled +1 more	Gnot provided
Select item 2350159	NM_032787.3(ADGRG7):c.335C>T (p.Ala112Val)	ADGRG7 (A112V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086996	NM_032787.3(ADGRG7):c.347T>C (p.Met116Thr)	ADGRG7 (M116T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087001	NM_032787.3(ADGRG7):c.355C>T (p.Arg119Trp)	ADGRG7 (R119W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087010	NM_032787.3(ADGRG7):c.356G>A (p.Arg119Gln)	ADGRG7 (R119Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087018	NM_032787.3(ADGRG7):c.443A>G (p.Lys148Arg)	ADGRG7 (K148R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087026	NM_032787.3(ADGRG7):c.523A>G (p.Thr175Ala)	ADGRG7 (T175A)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2345051	NM_032787.3(ADGRG7):c.548C>T (p.Thr183Met)	ADGRG7 (T183M)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3272010	NM_032787.3(ADGRG7):c.620C>G (p.Thr207Arg)	ADGRG7 (T207R)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3087051	NM_032787.3(ADGRG7):c.682G>T (p.Asp228Tyr)	ADGRG7 (D228Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 144848	GRCh38/hg38 3q12.2(chr3:100641848-100725206)x4	ADGRG7, LOC129937149 +2 more	Copy number gain	See cases	GBenign/Likely benign
Select item 144847	GRCh38/hg38 3q12.2(chr3:100641848-100725206)x5	ADGRG7, LOC129937149 +2 more	Copy number gain	See cases	GBenign
Select item 144846	GRCh38/hg38 3q12.2(chr3:100641848-100725206)x3	ADGRG7, LOC129937149 +2 more	Copy number gain	See cases	GBenign/Likely benign
Select item 2515093	NM_032787.3(ADGRG7):c.703A>G (p.Ile235Val)	ADGRG7 (I235V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529003	NM_032787.3(ADGRG7):c.704T>C (p.Ile235Thr)	ADGRG7 (I235T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254651	NM_032787.3(ADGRG7):c.748G>C (p.Val250Leu)	ADGRG7 (V250L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2241745	NM_032787.3(ADGRG7):c.751G>C (p.Val251Leu)	ADGRG7 (V251L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393565	NM_032787.3(ADGRG7):c.786C>A (p.Phe262Leu)	ADGRG7 (F262L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2408496	NM_032787.3(ADGRG7):c.820C>T (p.Arg274Cys)	ADGRG7 (R274C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272051	NM_032787.3(ADGRG7):c.832C>A (p.Gln278Lys)	ADGRG7 (Q278K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 738678	NM_032787.3(ADGRG7):c.839-7C>T	ADGRG7	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2286466	NM_032787.3(ADGRG7):c.874A>G (p.Ile292Val)	ADGRG7 (I292V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2622202	NM_032787.3(ADGRG7):c.957G>T (p.Lys319Asn)	ADGRG7 (K24N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249731	NM_032787.3(ADGRG7):c.977A>G (p.Tyr326Cys)	ADGRG7 (Y326C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087101	NM_032787.3(ADGRG7):c.991C>G (p.Leu331Val)	ADGRG7 (L331V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597449	NM_032787.3(ADGRG7):c.1022C>T (p.Ser341Leu)	ADGRG7 (S46L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287578	NM_032787.3(ADGRG7):c.1084T>G (p.Ser362Ala)	ADGRG7 (S362A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272062	NM_032787.3(ADGRG7):c.1136A>T (p.Tyr379Phe)	ADGRG7 (Y379F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272044	NM_032787.3(ADGRG7):c.1180G>C (p.Asp394His)	ADGRG7 (D99H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607582	NM_032787.3(ADGRG7):c.1190G>A (p.Gly397Asp)	ADGRG7 (G397D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339590	NM_032787.3(ADGRG7):c.1198A>G (p.Lys400Glu)	ADGRG7 (K400E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208334	NM_032787.3(ADGRG7):c.1232G>A (p.Arg411His)	ADGRG7 (R116H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2285188	NM_032787.3(ADGRG7):c.1250A>G (p.Asn417Ser)	ADGRG7 (N122S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325364	NM_032787.3(ADGRG7):c.1294A>C (p.Lys432Gln)	ADGRG7 (K432Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507839	NM_032787.3(ADGRG7):c.1316A>G (p.Asn439Ser)	ADGRG7 (N144S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377126	NM_032787.3(ADGRG7):c.1324T>A (p.Cys442Ser)	ADGRG7 (C442S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277424	NM_032787.3(ADGRG7):c.1331T>C (p.Leu444Pro)	ADGRG7 (L149P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407318	NM_032787.3(ADGRG7):c.1348G>A (p.Ala450Thr)	ADGRG7 (A155T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272003	NM_032787.3(ADGRG7):c.1380G>A (p.Arg460=)	ADGRG7	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3086922	NM_032787.3(ADGRG7):c.1408G>A (p.Val470Ile)	ADGRG7 (V470I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086927	NM_032787.3(ADGRG7):c.1488G>T (p.Leu496Phe)	ADGRG7 (L201F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272057	NM_032787.3(ADGRG7):c.1504G>A (p.Asp502Asn)	ADGRG7 (D502N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284911	NM_032787.3(ADGRG7):c.1573A>G (p.Met525Val)	ADGRG7 (M230V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344526	NM_032787.3(ADGRG7):c.1624A>C (p.Thr542Pro)	ADGRG7 (T542P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272019	NM_032787.3(ADGRG7):c.1633G>T (p.Ala545Ser)	ADGRG7 (A250S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494637	NM_032787.3(ADGRG7):c.1642G>A (p.Ala548Thr)	ADGRG7 (A548T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086935	NM_032787.3(ADGRG7):c.1677G>A (p.Met559Ile)	ADGRG7 (M559I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086938	NM_032787.3(ADGRG7):c.1691G>A (p.Arg564Gln)	ADGRG7 (R269Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2221711	NM_032787.3(ADGRG7):c.1716A>T (p.Leu572Phe)	ADGRG7 (L277F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 782808	NM_032787.3(ADGRG7):c.1794G>A (p.Gln598=)	ADGRG7	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2221150	NM_032787.3(ADGRG7):c.1810C>T (p.Arg604Trp)	ADGRG7 (R604W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2053239	NM_032787.3(ADGRG7):c.1845dup (p.Pro616fs)	ADGRG7 (P321fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 3086941	NM_032787.3(ADGRG7):c.1868C>T (p.Pro623Leu)	ADGRG7 (P623L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465388	NM_032787.3(ADGRG7):c.1877G>T (p.Trp626Leu)	ADGRG7 (W331L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330248	NM_032787.3(ADGRG7):c.1913G>A (p.Ser638Asn)	ADGRG7 (S343N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3272031	NM_032787.3(ADGRG7):c.1925T>G (p.Met642Arg)	ADGRG7 (M642R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595144	NM_032787.3(ADGRG7):c.2098G>T (p.Val700Phe)	ADGRG7 (V700F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086952	NM_032787.3(ADGRG7):c.2105G>A (p.Ser702Asn)	ADGRG7 (S702N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320511	NM_032787.3(ADGRG7):c.2122T>C (p.Phe708Leu)	ADGRG7 (F413L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315742	NM_032787.3(ADGRG7):c.2164G>C (p.Val722Leu)	ADGRG7 (V427L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086962	NM_032787.3(ADGRG7):c.2179T>G (p.Phe727Val)	ADGRG7 (F727V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 789990	NM_032787.3(ADGRG7):c.2191G>A (p.Ala731Thr)	ADGRG7 (A731T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3086965	NM_032787.3(ADGRG7):c.2232G>T (p.Arg744Ser)	ADGRG7 (R449S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086968	NM_032787.3(ADGRG7):c.2258C>T (p.Pro753Leu)	ADGRG7 (P753L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 716846	NM_032787.3(ADGRG7):c.2267G>A (p.Arg756His)	ADGRG7 (R461H +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2280610	NM_032787.3(ADGRG7):c.2302A>G (p.Thr768Ala)	ADGRG7 (T768A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 730290	NM_032787.3(ADGRG7):c.2303C>A (p.Thr768Asn)	ADGRG7 (T473N +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 730291	NM_032787.3(ADGRG7):c.2309A>G (p.His770Arg)	ADGRG7 (H770R +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 3086976	NM_032787.3(ADGRG7):c.2315G>A (p.Arg772His)	ADGRG7 (R477H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2392843	NM_032787.3(ADGRG7):c.2339C>T (p.Pro780Leu)	ADGRG7 (P780L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3086985	NM_032787.3(ADGRG7):c.2357C>T (p.Thr786Ile)	ADGRG7 (T491I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3247040	NC_000003.11:g.(?_99509527)_(101484395_?)del	ABI3BP, ADGRG7 +16 more	Deletion	not provided	GUncertain significance
Select item 3062743	GRCh37/hg19 3q11.1-12.3(chr3:93519465-101464485)x3	ABI3BP, ADGRG7 +41 more	Copy number gain	not specified	GUncertain significance
Select item 3062674	GRCh37/hg19 3q12.2-13.11(chr3:100369522-104621416)x1	ABI3BP, ADGRG7 +11 more	Copy number loss	not specified	GUncertain significance
Select item 980048	GRCh37/hg19 3q11.2-12.3(chr3:95563096-102371126)x1	OR5AC2, GPR15 +39 more	Copy number loss	not provided	GLikely pathogenic
Select item 442401	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)x3	HHLA2, HIGD1A +1054 more	Copy number gain	See cases	GPathogenic
Select item 442400	GRCh37/hg19 3p26.3-q29(chr3:61892-197851986)	A4GNT, AADAC +1054 more	Copy number gain	See cases	GPathogenic

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 91