ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 118
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 5q14.3(chr5:89858793-89914907)x3
NC_000005.10:g.90558508A>G
NC_000005.10:g.90558631G>C
NC_000005.10:g.90644923del
NC_000005.10:g.90651388_90651391del
NM_032119.4(ADGRV1):c.-47G>C
NM_032119.4(ADGRV1):c.10039T>C (p.Phe3347Leu) rs10067636
NM_032119.4(ADGRV1):c.10054-74A>G
NM_032119.4(ADGRV1):c.10161+218C>T
NM_032119.4(ADGRV1):c.10162-209T>C
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.10769+79G>A
NM_032119.4(ADGRV1):c.10769+9A>G rs116184119
NM_032119.4(ADGRV1):c.11122-153A>G
NM_032119.4(ADGRV1):c.11122-24C>T
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.11682C>T (p.Pro3894=) rs2438349
NM_032119.4(ADGRV1):c.11757+30A>G
NM_032119.4(ADGRV1):c.11940+78A>G
NM_032119.4(ADGRV1):c.11941-96C>A
NM_032119.4(ADGRV1):c.12121-121T>A
NM_032119.4(ADGRV1):c.1238+74A>T
NM_032119.4(ADGRV1):c.12528-332A>G
NM_032119.4(ADGRV1):c.12592G>A (p.Val4198Met) rs2460169
NM_032119.4(ADGRV1):c.12667-147G>T
NM_032119.4(ADGRV1):c.12850-36A>T
NM_032119.4(ADGRV1):c.13082+146C>G
NM_032119.4(ADGRV1):c.13232-268_13232-267dup
NM_032119.4(ADGRV1):c.13653+98C>T
NM_032119.4(ADGRV1):c.14029T>C (p.Phe4677Leu) rs62000408
NM_032119.4(ADGRV1):c.14515C>G (p.Gln4839Glu) rs79464236
NM_032119.4(ADGRV1):c.14905T>C (p.Trp4969Arg) rs7729495
NM_032119.4(ADGRV1):c.14972+231T>G
NM_032119.4(ADGRV1):c.1510-51C>A
NM_032119.4(ADGRV1):c.16196+147T>C
NM_032119.4(ADGRV1):c.16248C>T (p.Val5416=) rs3763073
NM_032119.4(ADGRV1):c.1652T>C (p.Val551Ala) rs6889939
NM_032119.4(ADGRV1):c.16949C>G (p.Thr5650Ser) rs61748627
NM_032119.4(ADGRV1):c.17594+210A>G
NM_032119.4(ADGRV1):c.1817A>C (p.Asn606Thr) rs61749567
NM_032119.4(ADGRV1):c.18310+175C>T
NM_032119.4(ADGRV1):c.1839+32G>A
NM_032119.4(ADGRV1):c.1839+54C>T
NM_032119.4(ADGRV1):c.2001T>C (p.Asp667=) rs9293547
NM_032119.4(ADGRV1):c.2016+53del
NM_032119.4(ADGRV1):c.22+56C>T
NM_032119.4(ADGRV1):c.2241-10A>T rs150996234
NM_032119.4(ADGRV1):c.2553+209G>A
NM_032119.4(ADGRV1):c.2734+236G>C
NM_032119.4(ADGRV1):c.2735-10C>A rs78625945
NM_032119.4(ADGRV1):c.2735-34C>G
NM_032119.4(ADGRV1):c.2898+85A>G
NM_032119.4(ADGRV1):c.2899-42T>C
NM_032119.4(ADGRV1):c.327C>T (p.Asp109=) rs61753944
NM_032119.4(ADGRV1):c.3289+118G>A
NM_032119.4(ADGRV1):c.3289+189T>G
NM_032119.4(ADGRV1):c.3289+191del
NM_032119.4(ADGRV1):c.3289+193A>T
NM_032119.4(ADGRV1):c.3289+194C>A
NM_032119.4(ADGRV1):c.3290-174C>T
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.358-216A>G
NM_032119.4(ADGRV1):c.380T>G (p.Leu127Arg) rs41311333
NM_032119.4(ADGRV1):c.4254T>C (p.Tyr1418=) rs149459739
NM_032119.4(ADGRV1):c.4506C>T (p.Pro1502=) rs17543819
NM_032119.4(ADGRV1):c.454-80G>T
NM_032119.4(ADGRV1):c.4752+89T>C
NM_032119.4(ADGRV1):c.4929+234G>A
NM_032119.4(ADGRV1):c.4929+87A>T
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.5444-281A>G
NM_032119.4(ADGRV1):c.5524+183T>A
NM_032119.4(ADGRV1):c.558+186T>C
NM_032119.4(ADGRV1):c.558+207T>G
NM_032119.4(ADGRV1):c.558+295G>C
NM_032119.4(ADGRV1):c.5665-23T>C rs4916683
NM_032119.4(ADGRV1):c.5747C>T (p.Thr1916Ile) rs35791889
NM_032119.4(ADGRV1):c.581C>A (p.Pro194His) rs61745498
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.6608T>C (p.Val2203Ala) rs200055351
NM_032119.4(ADGRV1):c.672+56T>C
NM_032119.4(ADGRV1):c.7079G>A (p.Arg2360His) rs111033470
NM_032119.4(ADGRV1):c.7133+48G>A
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.7813T>G (p.Leu2605Val) rs79915053
NM_032119.4(ADGRV1):c.7945+27C>A rs10068473
NM_032119.4(ADGRV1):c.8155+82T>C
NM_032119.4(ADGRV1):c.8287-238A>G
NM_032119.4(ADGRV1):c.8566+90C>T
NM_032119.4(ADGRV1):c.8567-289G>C
NM_032119.4(ADGRV1):c.8567-60G>T
NM_032119.4(ADGRV1):c.8691A>C (p.Glu2897Asp) rs201586455
NM_032119.4(ADGRV1):c.8730+9_8730+10del rs780180737
NM_032119.4(ADGRV1):c.8825-246T>G
NM_032119.4(ADGRV1):c.8876G>A (p.Arg2959Gln) rs73175207
NM_032119.4(ADGRV1):c.9042+149T>A
NM_032119.4(ADGRV1):c.9042+57C>T
NM_032119.4(ADGRV1):c.9366A>G (p.Thr3122=) rs200412477
NM_032119.4(ADGRV1):c.9447+157G>A
NM_032119.4(ADGRV1):c.9447+68A>T
NM_032119.4(ADGRV1):c.9448-73C>T
NM_032119.4(ADGRV1):c.9607T>A (p.Ser3203Thr) rs116480183
NM_032119.4(ADGRV1):c.9623+89A>G
NM_032119.4(ADGRV1):c.9771C>T (p.Ser3257=) rs16869039
NM_032119.4(ADGRV1):c.9907-35A>C rs7723259
NM_032119.4(ADGRV1):c.9927T>G (p.Pro3309=) rs16869042

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.