ClinVar Miner

List of variants in gene ADGRV1 reported as benign for not specified

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Gene type:
ClinVar version:
Total variants: 155
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HGVS dbSNP
NM_032119.4(ADGRV1):c.-44C>T rs192362302
NM_032119.4(ADGRV1):c.-98G>A
NM_032119.4(ADGRV1):c.10039T>C (p.Phe3347Leu) rs10067636
NM_032119.4(ADGRV1):c.10126A>G (p.Ile3376Val) rs200528472
NM_032119.4(ADGRV1):c.10339G>A (p.Glu3447Lys) rs397517419
NM_032119.4(ADGRV1):c.10411G>A (p.Glu3471Lys) rs2366928
NM_032119.4(ADGRV1):c.10577T>C (p.Met3526Thr) rs41311343
NM_032119.4(ADGRV1):c.10607G>A (p.Arg3536His) rs144618536
NM_032119.4(ADGRV1):c.10769+9A>G rs116184119
NM_032119.4(ADGRV1):c.10796G>C (p.Gly3599Ala) rs145294917
NM_032119.4(ADGRV1):c.1086A>G (p.Leu362=) rs186639101
NM_032119.4(ADGRV1):c.10872A>G (p.Gln3624=) rs17624033
NM_032119.4(ADGRV1):c.10936T>C (p.Ser3646Pro) rs13171868
NM_032119.4(ADGRV1):c.11031C>T (p.Asn3677=) rs75480336
NM_032119.4(ADGRV1):c.11115A>T (p.Ser3705=) rs138029547
NM_032119.4(ADGRV1):c.1131T>G (p.Ser377=) rs200435877
NM_032119.4(ADGRV1):c.11472G>A (p.Leu3824=) rs74327115
NM_032119.4(ADGRV1):c.11481T>C (p.Asp3827=) rs16869083
NM_032119.4(ADGRV1):c.11581-3dup rs34894132
NM_032119.4(ADGRV1):c.11599G>A (p.Glu3867Lys) rs10062026
NM_032119.4(ADGRV1):c.11682C>T (p.Pro3894=) rs2438349
NM_032119.4(ADGRV1):c.12269C>A (p.Thr4090Asn) rs199839743
NM_032119.4(ADGRV1):c.12476A>C (p.His4159Pro) rs200805176
NM_032119.4(ADGRV1):c.12592G>A (p.Val4198Met) rs2460169
NM_032119.4(ADGRV1):c.12927G>A (p.Ala4309=) rs35092519
NM_032119.4(ADGRV1):c.13037C>T (p.Pro4346Leu) rs74632023
NM_032119.4(ADGRV1):c.13232-7A>G rs2438358
NM_032119.4(ADGRV1):c.13590C>T (p.Pro4530=) rs41311745
NM_032119.4(ADGRV1):c.13599A>G (p.Thr4533=) rs17554631
NM_032119.4(ADGRV1):c.13654-5C>T rs367554300
NM_032119.4(ADGRV1):c.14029T>C (p.Phe4677Leu) rs62000408
NM_032119.4(ADGRV1):c.14309G>A (p.Arg4770His) rs41304892
NM_032119.4(ADGRV1):c.14466G>A (p.Val4822=) rs117641264
NM_032119.4(ADGRV1):c.14515C>G (p.Gln4839Glu) rs79464236
NM_032119.4(ADGRV1):c.14517+18A>G rs75316546
NM_032119.4(ADGRV1):c.14654A>G (p.Asn4885Ser) rs61731030
NM_032119.4(ADGRV1):c.14905T>C (p.Trp4969Arg) rs7729495
NM_032119.4(ADGRV1):c.14943G>C (p.Gln4981His) rs200153555
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.15786C>T (p.Phe5262=) rs369083434
NM_032119.4(ADGRV1):c.16031A>G (p.Glu5344Gly) rs2438374
NM_032119.4(ADGRV1):c.16164A>G (p.Arg5388=) rs41304884
NM_032119.4(ADGRV1):c.16248C>T (p.Val5416=) rs3763073
NM_032119.4(ADGRV1):c.16279G>A (p.Val5427Met) rs2438378
NM_032119.4(ADGRV1):c.16377G>T (p.Gln5459His) rs371947306
NM_032119.4(ADGRV1):c.1652T>C (p.Val551Ala) rs6889939
NM_032119.4(ADGRV1):c.16841C>T (p.Thr5614Ile) rs149544995
NM_032119.4(ADGRV1):c.16949C>G (p.Thr5650Ser) rs61748627
NM_032119.4(ADGRV1):c.17017A>G (p.Lys5673Glu) rs41303350
NM_032119.4(ADGRV1):c.17626G>A (p.Val5876Ile) rs2247870
NM_032119.4(ADGRV1):c.17735C>G (p.Ser5912Cys) rs146120983
NM_032119.4(ADGRV1):c.17856+11G>A rs187039736
NM_032119.4(ADGRV1):c.1817A>C (p.Asn606Thr) rs61749567
NM_032119.4(ADGRV1):c.18273A>G (p.Ala6091=) rs137853918
NM_032119.4(ADGRV1):c.18311-9dup rs140911567
NM_032119.4(ADGRV1):c.1839+7G>A rs142011700
NM_032119.4(ADGRV1):c.18433-16T>C rs72784680
NM_032119.4(ADGRV1):c.18433-17_18433-16insCT rs1554239805
NM_032119.4(ADGRV1):c.18433-5del rs35858094
NM_032119.4(ADGRV1):c.18470A>G (p.Asn6157Ser) rs200111522
NM_032119.4(ADGRV1):c.18475A>G (p.Met6159Val) rs77469944
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met) rs199988872
NM_032119.4(ADGRV1):c.18625-7= rs7726023
NM_032119.4(ADGRV1):c.18625-7T>C rs7726023
NM_032119.4(ADGRV1):c.18741G>A (p.Gly6247=) rs13158963
NM_032119.4(ADGRV1):c.18746T>G (p.Leu6249Arg) rs41311625
NM_032119.4(ADGRV1):c.18803-13A>G rs41305902
NM_032119.4(ADGRV1):c.18803-4G>T rs80335659
NM_032119.4(ADGRV1):c.2001T>C (p.Asp667=) rs9293547
NM_032119.4(ADGRV1):c.2112G>A (p.Pro704=) rs182990046
NM_032119.4(ADGRV1):c.22+9T>C rs368604803
NM_032119.4(ADGRV1):c.2241-10A>T rs150996234
NM_032119.4(ADGRV1):c.2241-19G>T rs1344030
NM_032119.4(ADGRV1):c.2367+8= rs2366773
NM_032119.4(ADGRV1):c.2367+8C>T rs2366773
NM_032119.4(ADGRV1):c.2553+11T>A rs73181640
NM_032119.4(ADGRV1):c.2735-10C>A rs78625945
NM_032119.4(ADGRV1):c.3141A>G (p.Ala1047=) rs950692
NM_032119.4(ADGRV1):c.3279= (p.Leu1093=) rs2366777
NM_032119.4(ADGRV1):c.3279G>T (p.Leu1093Phe) rs2366777
NM_032119.4(ADGRV1):c.327C>T (p.Asp109=) rs61753944
NM_032119.4(ADGRV1):c.3289G>A (p.Gly1097Ser) rs148097083
NM_032119.4(ADGRV1):c.3295A>G (p.Thr1099Ala) rs61754947
NM_032119.4(ADGRV1):c.3303A>G (p.Val1101=) rs80069610
NM_032119.4(ADGRV1):c.3482C>G (p.Ser1161Cys) rs147062294
NM_032119.4(ADGRV1):c.3559A>G (p.Ile1187Val) rs16868935
NM_032119.4(ADGRV1):c.380T>G (p.Leu127Arg) rs41311333
NM_032119.4(ADGRV1):c.3956G>A (p.Arg1319Gln) rs73181648
NM_032119.4(ADGRV1):c.4254T>C (p.Tyr1418=) rs149459739
NM_032119.4(ADGRV1):c.4260A>G (p.Glu1420=) rs61740119
NM_032119.4(ADGRV1):c.4506C>T (p.Pro1502=) rs17543819
NM_032119.4(ADGRV1):c.463A>G (p.Ile155Val) rs199873924
NM_032119.4(ADGRV1):c.4752+19G>T rs59737743
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.5304G>A (p.Glu1768=) rs41303346
NM_032119.4(ADGRV1):c.5346A>G (p.Gly1782=) rs10067298
NM_032119.4(ADGRV1):c.5525-7C>T rs137853919
NM_032119.4(ADGRV1):c.5747C>T (p.Thr1916Ile) rs35791889
NM_032119.4(ADGRV1):c.5780C>T (p.Thr1927Met) rs17544552
NM_032119.4(ADGRV1):c.581C>A (p.Pro194His) rs61745498
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.5851G>A (p.Val1951Ile) rs4916684
NM_032119.4(ADGRV1):c.5953A>G (p.Asn1985Asp) rs41303352
NM_032119.4(ADGRV1):c.5960C>T (p.Pro1987Leu) rs4916685
NM_032119.4(ADGRV1):c.6012G>T (p.Leu2004Phe) rs16868972
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.6187T>C (p.Leu2063=) rs75019370
NM_032119.4(ADGRV1):c.6289C>T (p.Arg2097Cys) rs16868974
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408
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.6608T>C (p.Val2203Ala) rs200055351
NM_032119.4(ADGRV1):c.6695A>G (p.Tyr2232Cys) rs10037067
NM_032119.4(ADGRV1):c.6951+13G>A rs143356203
NM_032119.4(ADGRV1):c.6952-10G>A rs10040165
NM_032119.4(ADGRV1):c.6994A>T (p.Ile2332Phe) rs193030567
NM_032119.4(ADGRV1):c.7034A>G (p.Asn2345Ser) rs2366926
NM_032119.4(ADGRV1):c.7079G>A (p.Arg2360His) rs111033470
NM_032119.4(ADGRV1):c.7176C>T (p.Ser2392=) rs111033452
NM_032119.4(ADGRV1):c.7179C>T (p.Asp2393=) rs111033429
NM_032119.4(ADGRV1):c.7206G>A (p.Glu2402=) rs16876822
NM_032119.4(ADGRV1):c.7229A>G (p.Tyr2410Cys) rs111033430
NM_032119.4(ADGRV1):c.7284T>C (p.Asn2428=) rs148932387
NM_032119.4(ADGRV1):c.7293C>T (p.Ala2431=) rs77791584
NM_032119.4(ADGRV1):c.746G>A (p.Arg249Lys) rs41303344
NM_032119.4(ADGRV1):c.7576A>G (p.Ile2526Val) rs75191159
NM_032119.4(ADGRV1):c.7582C>T (p.Pro2528Ser) rs201733037
NM_032119.4(ADGRV1):c.7751A>G (p.Asn2584Ser) rs1878878
NM_032119.4(ADGRV1):c.7813T>G (p.Leu2605Val) rs79915053
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.8172C>T (p.Phe2724=) rs371019516
NM_032119.4(ADGRV1):c.8291C>T (p.Ser2764Leu) rs16869016
NM_032119.4(ADGRV1):c.8407G>A (p.Ala2803Thr) rs111033530
NM_032119.4(ADGRV1):c.8538T>G (p.Leu2846=) rs6880570
NM_032119.4(ADGRV1):c.8567-13C>T rs75881968
NM_032119.4(ADGRV1):c.8691A>C (p.Glu2897Asp) rs201586455
NM_032119.4(ADGRV1):c.8730+10_8730+11insC rs377585302
NM_032119.4(ADGRV1):c.8730+9C>T rs886043931
NM_032119.4(ADGRV1):c.8730+9_8730+10del rs780180737
NM_032119.4(ADGRV1):c.8876G>A (p.Arg2959Gln) rs73175207
NM_032119.4(ADGRV1):c.9213C>T (p.Asp3071=) rs56329646
NM_032119.4(ADGRV1):c.9280G>A (p.Val3094Ile) rs13157270
NM_032119.4(ADGRV1):c.9366A>G (p.Thr3122=) rs200412477
NM_032119.4(ADGRV1):c.9607T>A (p.Ser3203Thr) rs116480183
NM_032119.4(ADGRV1):c.9650C>T (p.Ala3217Val) rs114137750
NM_032119.4(ADGRV1):c.9743G>A (p.Gly3248Asp) rs16869032
NM_032119.4(ADGRV1):c.9771C>T (p.Ser3257=) rs16869039
NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=) rs16869042

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