"Ambry Genetics"[submitter] AND "ADGRL2"[gene] - ClinVar

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Items: 69

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2589260	NM_001366006.2(ADGRL2):c.8C>T (p.Ser3Phe)	ADGRL2 (S3F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087570	NM_001366006.2(ADGRL2):c.44T>C (p.Ile15Thr)	ADGRL2 (I15T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296825	NM_001366006.2(ADGRL2):c.94C>G (p.Pro32Ala)	ADGRL2 (P32A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336246	NM_001366006.2(ADGRL2):c.145C>G (p.Leu49Val)	ADGRL2 (L49V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2383240	NM_001366006.2(ADGRL2):c.175A>G (p.Ile59Val)	ADGRL2 (I59V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2297309	NM_001366006.2(ADGRL2):c.288G>T (p.Arg96Ser)	ADGRL2 (R96S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2326681	NM_001366006.2(ADGRL2):c.571G>T (p.Ala191Ser)	ADGRL2 (A187S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2300944	NM_001366006.2(ADGRL2):c.613T>C (p.Tyr205His)	ADGRL2 (Y205H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617335	NM_001366006.2(ADGRL2):c.905T>A (p.Phe302Tyr)	ADGRL2 (F302Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087408	NM_001366006.2(ADGRL2):c.1105A>G (p.Ile369Val)	ADGRL2 (I369V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607992	NM_001366006.2(ADGRL2):c.1157A>G (p.Asn386Ser)	ADGRL2 (N386S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2229293	NM_001366006.2(ADGRL2):c.1177T>C (p.Ser393Pro)	ADGRL2 (S389P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525856	NM_001366006.2(ADGRL2):c.1204G>A (p.Ala402Thr)	ADGRL2 (A398T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464096	NM_001366006.2(ADGRL2):c.1249C>G (p.Leu417Val)	ADGRL2 (L413V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272274	NM_001366006.2(ADGRL2):c.1261A>G (p.Ile421Val)	ADGRL2 (I417V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456722	NM_001366006.2(ADGRL2):c.1268C>T (p.Ser423Leu)	ADGRL2 (S419L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272253	NM_001366006.2(ADGRL2):c.1282A>G (p.Thr428Ala)	ADGRL2 (T428A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225217	NM_001366006.2(ADGRL2):c.1288C>G (p.Gln430Glu)	ADGRL2 (Q430E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483413	NM_001366006.2(ADGRL2):c.1361T>C (p.Val454Ala)	ADGRL2 (V450A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087438	NM_001366006.2(ADGRL2):c.1519C>T (p.Leu507Phe)	ADGRL2 (L503F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087441	NM_001366006.2(ADGRL2):c.1525A>G (p.Met509Val)	ADGRL2 (M505V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615819	NM_001366006.2(ADGRL2):c.1552A>G (p.Lys518Glu)	ADGRL2 (K518E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2607273	NM_001366006.2(ADGRL2):c.1574G>A (p.Cys525Tyr)	ADGRL2 (C521Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2207896	NM_001366006.2(ADGRL2):c.1699G>A (p.Val567Met)	ADGRL2 (V563M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087459	NM_001366006.2(ADGRL2):c.1913C>G (p.Ala638Gly)	ADGRL2 (A638G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087463	NM_001366006.2(ADGRL2):c.2015T>C (p.Ile672Thr)	ADGRL2 (I655T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231793	NM_001366006.2(ADGRL2):c.2032G>T (p.Val678Leu)	ADGRL2 (V661L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209603	NM_001366006.2(ADGRL2):c.2077G>A (p.Gly693Ser)	ADGRL2 (G676S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307490	NM_001366006.2(ADGRL2):c.2113G>A (p.Ala705Thr)	ADGRL2 (A688T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272326	NM_001366006.2(ADGRL2):c.2409G>A (p.Met803Ile)	ADGRL2 (M799I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457518	NM_001366006.2(ADGRL2):c.2465C>T (p.Thr822Met)	ADGRL2 (T805M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087486	NM_001366006.2(ADGRL2):c.2594G>C (p.Cys865Ser)	ADGRL2 (C848S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329581	NM_001366006.2(ADGRL2):c.2641A>G (p.Ser881Gly)	ADGRL2 (S881G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087494	NM_001366006.2(ADGRL2):c.2672G>C (p.Cys891Ser)	ADGRL2 (C874S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272314	NM_001366006.2(ADGRL2):c.2701T>A (p.Phe901Ile)	ADGRL2 (F884I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272264	NM_001366006.2(ADGRL2):c.2748A>G (p.Ile916Met)	ADGRL2 (I899M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272320	NM_001366006.2(ADGRL2):c.2752G>C (p.Ala918Pro)	ADGRL2 (A901P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294710	NM_001366006.2(ADGRL2):c.2773T>A (p.Phe925Ile)	ADGRL2 (F908I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087499	NM_001366006.2(ADGRL2):c.2866T>A (p.Tyr956Asn)	ADGRL2 (Y939N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2250260	NM_001366006.2(ADGRL2):c.2917G>A (p.Ala973Thr)	ADGRL2 (A956T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346600	NM_001366006.2(ADGRL2):c.2966A>G (p.His989Arg)	ADGRL2 (H985R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302915	NM_001366006.2(ADGRL2):c.2996T>C (p.Ile999Thr)	ADGRL2 (I999T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272307	NM_001366006.2(ADGRL2):c.3058A>G (p.Met1020Val)	ADGRL2 (M1003V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535313	NM_001366006.2(ADGRL2):c.3065A>C (p.Lys1022Thr)	ADGRL2 (K1018T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2481672	NM_001366006.2(ADGRL2):c.3092C>G (p.Ser1031Cys)	ADGRL2 (S1027C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484197	NM_001366006.2(ADGRL2):c.3122T>G (p.Val1041Gly)	ADGRL2 (V1024G +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3272334	NM_001366006.2(ADGRL2):c.3211T>C (p.Tyr1071His)	ADGRL2 (Y1086H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336590	NM_001366006.2(ADGRL2):c.3269C>T (p.Ala1090Val)	ADGRL2 (A1073V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493442	NM_001366006.2(ADGRL2):c.3334C>T (p.Leu1112Phe)	ADGRL2 (L1095F +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087523	NM_001366006.2(ADGRL2):c.3392G>A (p.Arg1131His)	ADGRL2 (R1114H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087528	NM_001366006.2(ADGRL2):c.3398C>A (p.Ser1133Tyr)	ADGRL2 (S1116Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2242569	NM_001366006.2(ADGRL2):c.3466T>G (p.Phe1156Val)	ADGRL2 (F1171V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2211903	NM_001366006.2(ADGRL2):c.3485A>G (p.Asn1162Ser)	ADGRL2 (N1158S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3272285	NM_001366006.2(ADGRL2):c.3740A>G (p.His1247Arg)	ADGRL2 (H1194R +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3272296	NM_001366006.2(ADGRL2):c.3744G>C (p.Lys1248Asn)	ADGRL2 (K1248N +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2622229	NM_001366006.2(ADGRL2):c.3763G>C (p.Val1255Leu)	ADGRL2 (V1249L +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2289056	NM_001366006.2(ADGRL2):c.3763G>A (p.Val1255Met)	ADGRL2 (V1249M +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2323717	NM_001366006.2(ADGRL2):c.3779G>A (p.Cys1260Tyr)	ADGRL2 (C1254Y +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2383271	NM_001366006.2(ADGRL2):c.3790C>A (p.Leu1264Met)	ADGRL2 (L1211M +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2316722	NM_001366006.2(ADGRL2):c.3847C>T (p.Arg1283Trp)	ADGRL2 (R1217W +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2411932	NM_001366006.2(ADGRL2):c.3895C>T (p.Pro1299Ser)	ADGRL2 (P1233S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2309121	NM_001366006.2(ADGRL2):c.3956T>C (p.Met1319Thr)	ADGRL2 (M1313T +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2249811	NM_001366006.2(ADGRL2):c.4009C>A (p.Leu1337Ile)	ADGRL2 (L1284I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2521199	NM_001366006.2(ADGRL2):c.4070G>A (p.Gly1357Glu)	ADGRL2 (G1304E +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3087560	NM_001366006.2(ADGRL2):c.4114C>T (p.His1372Tyr)	ADGRL2 (H1372Y +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3087561	NM_001366006.2(ADGRL2):c.4137C>A (p.Asp1379Glu)	ADGRL2 (D1379E +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2288798	NM_001366006.2(ADGRL2):c.4258A>G (p.Met1420Val)	ADGRL2 (M1420V +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3087564	NM_001366006.2(ADGRL2):c.4328A>G (p.Tyr1443Cys)	ADGRL2 (Y1377C +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3087566	NM_001366006.2(ADGRL2):c.4377A>T (p.Arg1459Ser)	ADGRL2 (R1453S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 69