"Ambry Genetics"[submitter] AND "ADGRG7"[gene] - ClinVar

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Items: 67

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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 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 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 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 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

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Items: 67