ClinVar Miner

List of variants in gene ADGRV1 reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP
NM_032119.4(ADGRV1):c.10126A>G (p.Ile3376Val) rs200528472
NM_032119.4(ADGRV1):c.10162-272G>A
NM_032119.4(ADGRV1):c.10260C>T (p.Phe3420=) rs113938044
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.10550-7C>T rs191228562
NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=) rs200946170
NM_032119.4(ADGRV1):c.1056G>A (p.Pro352=) rs115239207
NM_032119.4(ADGRV1):c.10614A>G (p.Gln3538=) rs182626712
NM_032119.4(ADGRV1):c.10620T>G (p.Ser3540=) rs775321108
NM_032119.4(ADGRV1):c.10769+9A>G rs116184119
NM_032119.4(ADGRV1):c.1086A>G (p.Leu362=) rs186639101
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.1131T>G (p.Ser377=) rs200435877
NM_032119.4(ADGRV1):c.1140A>G (p.Gln380=) rs373902384
NM_032119.4(ADGRV1):c.11568T>C (p.Val3856=) rs143004930
NM_032119.4(ADGRV1):c.11595A>G (p.Glu3865=)
NM_032119.4(ADGRV1):c.11941-24_11941-5del rs1554106202
NM_032119.4(ADGRV1):c.11941-4A>G rs1057521591
NM_032119.4(ADGRV1):c.12516C>T (p.Thr4172=) rs776057320
NM_032119.4(ADGRV1):c.12978A>G (p.Ala4326=)
NM_032119.4(ADGRV1):c.13037C>T (p.Pro4346Leu) rs74632023
NM_032119.4(ADGRV1):c.13227C>T (p.Phe4409=)
NM_032119.4(ADGRV1):c.13434-6A>G rs1057521453
NM_032119.4(ADGRV1):c.14373T>A (p.Ala4791=) rs375062187
NM_032119.4(ADGRV1):c.1522A>C (p.Ile508Leu) rs61744480
NM_032119.4(ADGRV1):c.15343C>T (p.Leu5115=) rs41304886
NM_032119.4(ADGRV1):c.15608A>G (p.Glu5203Gly) rs202106463
NM_032119.4(ADGRV1):c.15750G>T (p.Gly5250=) rs1554125056
NM_032119.4(ADGRV1):c.16175T>C (p.Ile5392Thr)
NM_032119.4(ADGRV1):c.16196+40T>C
NM_032119.4(ADGRV1):c.16308C>A (p.Thr5436=) rs137853917
NM_032119.4(ADGRV1):c.16312A>G (p.Thr5438Ala) rs201890097
NM_032119.4(ADGRV1):c.16377G>T (p.Gln5459His) rs371947306
NM_032119.4(ADGRV1):c.16436A>G (p.Asn5479Ser) rs368738607
NM_032119.4(ADGRV1):c.17735C>G (p.Ser5912Cys) rs146120983
NM_032119.4(ADGRV1):c.17756-5T>C rs148654550
NM_032119.4(ADGRV1):c.1776C>A (p.Val592=) rs184127858
NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=) rs137853918
NM_032119.4(ADGRV1):c.18433-4G>T
NM_032119.4(ADGRV1):c.18435A>T (p.Gly6145=)
NM_032119.4(ADGRV1):c.18803-4G>T rs80335659
NM_032119.4(ADGRV1):c.18903C>T (p.Ile6301=) rs776454298
NM_032119.4(ADGRV1):c.2017-5A>G rs763411569
NM_032119.4(ADGRV1):c.2119A>T (p.Ile707Leu) rs200897149
NM_032119.4(ADGRV1):c.2241-10A>T rs150996234
NM_032119.4(ADGRV1):c.3151G>T (p.Asp1051Tyr) rs145556097
NM_032119.4(ADGRV1):c.3191A>C (p.Glu1064Ala) rs190922596
NM_032119.4(ADGRV1):c.3255T>C (p.Asp1085=) rs183447491
NM_032119.4(ADGRV1):c.3482C>G (p.Ser1161Cys) rs147062294
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.5214A>G (p.Glu1738=) rs1554079073
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.6318G>A (p.Ala2106=) rs190981860
NM_032119.4(ADGRV1):c.6383G>A (p.Arg2128Gln) rs149390094
NM_032119.4(ADGRV1):c.6489T>C (p.Ala2163=) rs746331284
NM_032119.4(ADGRV1):c.6707-329G>T
NM_032119.4(ADGRV1):c.7079G>A (p.Arg2360His) rs111033470
NM_032119.4(ADGRV1):c.7155G>T (p.Leu2385=)
NM_032119.4(ADGRV1):c.7582C>T (p.Pro2528Ser) rs201733037
NM_032119.4(ADGRV1):c.7806C>G (p.Pro2602=) rs200241260
NM_032119.4(ADGRV1):c.7874G>A (p.Arg2625His) rs201214794
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.8730+9_8730+10del rs780180737
NM_032119.4(ADGRV1):c.8784A>T (p.Gly2928=) rs955913647
NM_032119.4(ADGRV1):c.9213C>T (p.Asp3071=) rs56329646
NM_032119.4(ADGRV1):c.9324A>C (p.Ala3108=) rs1554092817
NM_032119.4(ADGRV1):c.9496T>G (p.Tyr3166Asp) rs371646432
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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