ClinVar Miner

List of variants in gene ADGRV1 reported by Athena Diagnostics Inc

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Gene type:
ClinVar version:
Total variants: 76
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HGVS dbSNP
NM_032119.4(ADGRV1):c.10039T>C (p.Phe3347Leu) rs10067636
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+9A>G rs116184119
NM_032119.4(ADGRV1):c.10801A>G (p.Arg3601Gly)
NM_032119.4(ADGRV1):c.10872A>G (p.Gln3624=) rs17624033
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.11805C>T (p.Asn3935=) rs144269892
NM_032119.4(ADGRV1):c.11974G>A (p.Asp3992Asn) rs201386977
NM_032119.4(ADGRV1):c.12128T>C (p.Ile4043Thr) rs375632680
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.12349C>T (p.Arg4117Cys) rs138908576
NM_032119.4(ADGRV1):c.12527+6G>T rs141701016
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.12979G>A (p.Gly4327Arg) rs1251839466
NM_032119.4(ADGRV1):c.13590C>T (p.Pro4530=) rs41311745
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.14515C>G (p.Gln4839Glu) rs79464236
NM_032119.4(ADGRV1):c.14905T>C (p.Trp4969Arg) rs7729495
NM_032119.4(ADGRV1):c.15177G>T (p.Gln5059His) rs201416399
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.17108G>A (p.Arg5703His) rs201073459
NM_032119.4(ADGRV1):c.17314C>T (p.Arg5772Ter) rs749956288
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.18879C>T (p.Ile6293=) rs372350188
NM_032119.4(ADGRV1):c.2001T>C (p.Asp667=) rs9293547
NM_032119.4(ADGRV1):c.207+3A>G rs142356935
NM_032119.4(ADGRV1):c.22+9T>C rs368604803
NM_032119.4(ADGRV1):c.2241-10A>T rs150996234
NM_032119.4(ADGRV1):c.2307T>A (p.Asn769Lys)
NM_032119.4(ADGRV1):c.2735-10C>A rs78625945
NM_032119.4(ADGRV1):c.327C>T (p.Asp109=) rs61753944
NM_032119.4(ADGRV1):c.3295A>G (p.Thr1099Ala) rs61754947
NM_032119.4(ADGRV1):c.3443G>A (p.Gly1148Asp) rs200945405
NM_032119.4(ADGRV1):c.3509A>G (p.Tyr1170Cys) rs188772875
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.4786G>A (p.Val1596Ile)
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.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.7079G>A (p.Arg2360His) rs111033470
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.7873C>T (p.Arg2625Cys) rs201583659
NM_032119.4(ADGRV1):c.8088G>A (p.Leu2696=) rs373069459
NM_032119.4(ADGRV1):c.8401G>A (p.Gly2801Arg) rs760510612
NM_032119.4(ADGRV1):c.8407G>A (p.Ala2803Thr) rs111033530
NM_032119.4(ADGRV1):c.853C>G (p.Arg285Gly) rs200197273
NM_032119.4(ADGRV1):c.8572A>G (p.Ile2858Val) rs41308297
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.8876G>A (p.Arg2959Gln) rs73175207
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.9771C>T (p.Ser3257=) rs16869039

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