ClinVar Miner

List of variants in gene ADGRV1 reported as likely benign for not provided

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Total variants: 64
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HGVS dbSNP
GRCh37/hg19 5q14.3(chr5:89994983-90126770)x1
NM_032119.4(ADGRV1):c.10162-272G>A
NM_032119.4(ADGRV1):c.1033C>A (p.Gln345Lys) rs201236317
NM_032119.4(ADGRV1):c.10427-288T>C
NM_032119.4(ADGRV1):c.10549+306G>A
NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=) rs200946170
NM_032119.4(ADGRV1):c.10614A>G (p.Gln3538=) rs182626712
NM_032119.4(ADGRV1):c.10769+9A>G rs116184119
NM_032119.4(ADGRV1):c.10936T>C (p.Ser3646Pro) rs13171868
NM_032119.4(ADGRV1):c.11115A>T (p.Ser3705=) rs138029547
NM_032119.4(ADGRV1):c.11122-234G>A
NM_032119.4(ADGRV1):c.11595A>G (p.Glu3865=)
NM_032119.4(ADGRV1):c.11805C>T (p.Asn3935=) rs144269892
NM_032119.4(ADGRV1):c.12207C>T (p.Thr4069=) rs202066007
NM_032119.4(ADGRV1):c.12269C>A (p.Thr4090Asn) rs199839743
NM_032119.4(ADGRV1):c.12527+6G>T rs141701016
NM_032119.4(ADGRV1):c.12978A>G (p.Ala4326=)
NM_032119.4(ADGRV1):c.13227C>T (p.Phe4409=)
NM_032119.4(ADGRV1):c.14157A>G (p.Leu4719=) rs779582048
NM_032119.4(ADGRV1):c.14309G>A (p.Arg4770His) rs41304892
NM_032119.4(ADGRV1):c.15608A>G (p.Glu5203Gly) rs202106463
NM_032119.4(ADGRV1):c.16175T>C (p.Ile5392Thr)
NM_032119.4(ADGRV1):c.16196+40T>C
NM_032119.4(ADGRV1):c.16312A>G (p.Thr5438Ala) rs201890097
NM_032119.4(ADGRV1):c.17017A>G (p.Lys5673Glu) rs41303350
NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=) rs137853918
NM_032119.4(ADGRV1):c.1839+7G>A rs142011700
NM_032119.4(ADGRV1):c.18433-4G>T
NM_032119.4(ADGRV1):c.18435A>T (p.Gly6145=)
NM_032119.4(ADGRV1):c.18879C>T (p.Ile6293=) rs372350188
NM_032119.4(ADGRV1):c.22+9T>C rs368604803
NM_032119.4(ADGRV1):c.2456G>A (p.Ser819Asn) rs182395524
NM_032119.4(ADGRV1):c.3559A>G (p.Ile1187Val) rs16868935
NM_032119.4(ADGRV1):c.4128C>T (p.Asp1376=)
NM_032119.4(ADGRV1):c.4214C>T (p.Ser1405Phe) rs41305898
NM_032119.4(ADGRV1):c.4227C>T (p.Tyr1409=)
NM_032119.4(ADGRV1):c.4264A>G (p.Ser1422Gly)
NM_032119.4(ADGRV1):c.4487A>G (p.Tyr1496Cys) rs376401006
NM_032119.4(ADGRV1):c.4864T>C (p.Tyr1622His) rs111753827
NM_032119.4(ADGRV1):c.4939A>G (p.Ile1647Val) rs72782753
NM_032119.4(ADGRV1):c.564G>T (p.Glu188Asp)
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.6095C>T (p.Ala2032Val) rs142013761
NM_032119.4(ADGRV1):c.6133G>A (p.Gly2045Arg) rs41308846
NM_032119.4(ADGRV1):c.6559A>G (p.Ile2187Val) rs200512504
NM_032119.4(ADGRV1):c.6608T>C (p.Val2203Ala) rs200055351
NM_032119.4(ADGRV1):c.6707-329G>T
NM_032119.4(ADGRV1):c.7155G>T (p.Leu2385=)
NM_032119.4(ADGRV1):c.7284T>C (p.Asn2428=) rs148932387
NM_032119.4(ADGRV1):c.746G>A (p.Arg249Lys) rs41303344
NM_032119.4(ADGRV1):c.7582C>T (p.Pro2528Ser) rs201733037
NM_032119.4(ADGRV1):c.7874G>A (p.Arg2625His) rs201214794
NM_032119.4(ADGRV1):c.7945+6C>T rs139278305
NM_032119.4(ADGRV1):c.8088G>A (p.Leu2696=) rs373069459
NM_032119.4(ADGRV1):c.8133C>T (p.Ser2711=) rs116446814
NM_032119.4(ADGRV1):c.8161A>G (p.Ile2721Val) rs201963060
NM_032119.4(ADGRV1):c.8407G>A (p.Ala2803Thr) rs111033530
NM_032119.4(ADGRV1):c.8805T>G (p.Thr2935=) rs1561569406
NM_032119.4(ADGRV1):c.9607T>A (p.Ser3203Thr) rs116480183
NM_032119.4(ADGRV1):c.9624-78del
NM_032119.4(ADGRV1):c.9624-80del
NM_032119.4(ADGRV1):c.9635T>C (p.Ile3212Thr) rs199833843
NM_032119.4(ADGRV1):c.9642C>T (p.Ile3214=) rs778864521
NM_032119.4(ADGRV1):c.9650C>T (p.Ala3217Val) rs114137750

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