ClinVar Miner

Variants in gene ADGRV1 with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 123
Download table as spreadsheet
HGVS dbSNP
NM_032119.4(ADGRV1):c.10066A>G (p.Ile3356Val) rs727503078
NM_032119.4(ADGRV1):c.10149C>T (p.Ser3383=) rs376298949
NM_032119.4(ADGRV1):c.10228G>A (p.Val3410Met)
NM_032119.4(ADGRV1):c.10260C>T (p.Phe3420=) rs113938044
NM_032119.4(ADGRV1):c.10323G>T (p.Gly3441=) rs373354231
NM_032119.4(ADGRV1):c.1033C>A (p.Gln345Lys) rs201236317
NM_032119.4(ADGRV1):c.10342G>A (p.Val3448Met) rs199715642
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.11157C>A (p.Ile3719=) rs762094907
NM_032119.4(ADGRV1):c.11201T>C (p.Val3734Ala) rs113498662
NM_032119.4(ADGRV1):c.1140A>G (p.Gln380=) rs373902384
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.12212G>A (p.Arg4071Gln) rs202190568
NM_032119.4(ADGRV1):c.12349C>T (p.Arg4117Cys) rs138908576
NM_032119.4(ADGRV1):c.12350G>A (p.Arg4117His) rs202067248
NM_032119.4(ADGRV1):c.12463C>T (p.Pro4155Ser) rs576429729
NM_032119.4(ADGRV1):c.12527+6G>T rs141701016
NM_032119.4(ADGRV1):c.12586C>T (p.Pro4196Ser) rs397517420
NM_032119.4(ADGRV1):c.12721G>A (p.Ala4241Thr) rs727504627
NM_032119.4(ADGRV1):c.1292C>T (p.Ala431Val) rs111723628
NM_032119.4(ADGRV1):c.13496G>A (p.Arg4499His) rs375122809
NM_032119.4(ADGRV1):c.13579A>G (p.Ile4527Val) rs777190245
NM_032119.4(ADGRV1):c.13654-7C>T rs373551551
NM_032119.4(ADGRV1):c.13765G>A (p.Val4589Met) rs375258567
NM_032119.4(ADGRV1):c.14373T>A (p.Ala4791=) rs375062187
NM_032119.4(ADGRV1):c.14405G>A (p.Arg4802Gln) rs534266547
NM_032119.4(ADGRV1):c.14432C>T (p.Pro4811Leu) rs201747452
NM_032119.4(ADGRV1):c.14761G>A (p.Ala4921Thr) rs200115167
NM_032119.4(ADGRV1):c.14931A>G (p.Leu4977=) rs760841840
NM_032119.4(ADGRV1):c.14970C>A (p.Leu4990=) rs368420512
NM_032119.4(ADGRV1):c.15113T>C (p.Ile5038Thr) rs192561791
NM_032119.4(ADGRV1):c.15177G>T (p.Gln5059His) rs201416399
NM_032119.4(ADGRV1):c.1522A>C (p.Ile508Leu) rs61744480
NM_032119.4(ADGRV1):c.15608A>G (p.Glu5203Gly) rs202106463
NM_032119.4(ADGRV1):c.15987C>T (p.Tyr5329=) rs142097643
NM_032119.4(ADGRV1):c.16175T>C (p.Ile5392Thr) rs113837859
NM_032119.4(ADGRV1):c.16248C>G (p.Val5416=) rs3763073
NM_032119.4(ADGRV1):c.16285G>A (p.Glu5429Lys) rs183851734
NM_032119.4(ADGRV1):c.16312A>G (p.Thr5438Ala) rs201890097
NM_032119.4(ADGRV1):c.16436A>G (p.Asn5479Ser) rs368738607
NM_032119.4(ADGRV1):c.16699G>A (p.Val5567Ile) rs201677553
NM_032119.4(ADGRV1):c.16999A>G (p.Met5667Val) rs201767389
NM_032119.4(ADGRV1):c.17388G>A (p.Gln5796=) rs183208875
NM_032119.4(ADGRV1):c.17512G>A (p.Val5838Ile) rs727504913
NM_032119.4(ADGRV1):c.17613G>A (p.Gln5871=) rs371091564
NM_032119.4(ADGRV1):c.17758C>A (p.Leu5920Ile) rs202110635
NM_032119.4(ADGRV1):c.1776C>A (p.Val592=) rs184127858
NM_032119.4(ADGRV1):c.17973+7A>G rs751094041
NM_032119.4(ADGRV1):c.1797A>T (p.Arg599Ser) rs200058876
NM_032119.4(ADGRV1):c.17987G>T (p.Trp5996Leu) rs544077645
NM_032119.4(ADGRV1):c.18144T>C (p.His6048=) rs188017433
NM_032119.4(ADGRV1):c.18349G>A (p.Val6117Met) rs200062593
NM_032119.4(ADGRV1):c.1837C>A (p.Gln613Lys) rs199587998
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met) rs199988872
NM_032119.4(ADGRV1):c.1855T>G (p.Leu619Val) rs202064612
NM_032119.4(ADGRV1):c.18746T>G (p.Leu6249Arg) rs41311625
NM_032119.4(ADGRV1):c.18879C>T (p.Ile6293=) rs372350188
NM_032119.4(ADGRV1):c.2023A>C (p.Ile675Leu) rs200187681
NM_032119.4(ADGRV1):c.207+3A>G rs142356935
NM_032119.4(ADGRV1):c.2106G>A (p.Val702=) rs749630454
NM_032119.4(ADGRV1):c.2112G>A (p.Pro704=) rs182990046
NM_032119.4(ADGRV1):c.21A>C (p.Pro7=) rs727504831
NM_032119.4(ADGRV1):c.222C>T (p.Asp74=) rs181146384
NM_032119.4(ADGRV1):c.2459A>G (p.Asn820Ser) rs144918959
NM_032119.4(ADGRV1):c.2538G>A (p.Leu846=) rs375415491
NM_032119.4(ADGRV1):c.2596C>T (p.Arg866Trp) rs200389929
NM_032119.4(ADGRV1):c.267C>T (p.Ala89=) rs759771981
NM_032119.4(ADGRV1):c.2734+8A>G rs371906040
NM_032119.4(ADGRV1):c.2740T>C (p.Tyr914His) rs189967386
NM_032119.4(ADGRV1):c.2759G>A (p.Arg920Gln) rs766225545
NM_032119.4(ADGRV1):c.2820A>G (p.Val940=) rs369910075
NM_032119.4(ADGRV1):c.3022+8T>C rs375286987
NM_032119.4(ADGRV1):c.3151G>T (p.Asp1051Tyr) rs145556097
NM_032119.4(ADGRV1):c.3443G>A (p.Gly1148Asp) rs200945405
NM_032119.4(ADGRV1):c.357+8C>T rs376004946
NM_032119.4(ADGRV1):c.3819G>A (p.Arg1273=) rs764738838
NM_032119.4(ADGRV1):c.4032C>T (p.Tyr1344=) rs376636949
NM_032119.4(ADGRV1):c.4214C>T (p.Ser1405Phe) rs41305898
NM_032119.4(ADGRV1):c.4264A>G (p.Ser1422Gly) rs377136573
NM_032119.4(ADGRV1):c.4349A>G (p.Lys1450Arg) rs372188446
NM_032119.4(ADGRV1):c.4487A>G (p.Tyr1496Cys) rs376401006
NM_032119.4(ADGRV1):c.466G>A (p.Ala156Thr) rs201180985
NM_032119.4(ADGRV1):c.5072C>T (p.Thr1691Met) rs146954342
NM_032119.4(ADGRV1):c.5221T>C (p.Leu1741=) rs371831553
NM_032119.4(ADGRV1):c.5282C>G (p.Ser1761Cys) rs200392821
NM_032119.4(ADGRV1):c.5576A>G (p.His1859Arg) rs200974394
NM_032119.4(ADGRV1):c.564G>T (p.Glu188Asp) rs377529304
NM_032119.4(ADGRV1):c.5658A>G (p.Thr1886=) rs377468788
NM_032119.4(ADGRV1):c.5785G>T (p.Ala1929Ser) rs41311335
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.5953A>C (p.Asn1985His) rs41303352
NM_032119.4(ADGRV1):c.6242C>G (p.Ser2081Cys) rs201210744
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408
NM_032119.4(ADGRV1):c.6443C>T (p.Ala2148Val) rs375921325
NM_032119.4(ADGRV1):c.6559A>G (p.Ile2187Val) rs200512504
NM_032119.4(ADGRV1):c.6684T>A (p.Ser2228=) rs373667458
NM_032119.4(ADGRV1):c.684T>C (p.Asn228=) rs181889432
NM_032119.4(ADGRV1):c.6994A>T (p.Ile2332Phe) rs193030567
NM_032119.4(ADGRV1):c.705A>G (p.Gln235=) rs372853480
NM_032119.4(ADGRV1):c.7294G>A (p.Val2432Met) rs111033531
NM_032119.4(ADGRV1):c.7569A>G (p.Thr2523=) rs373352597
NM_032119.4(ADGRV1):c.7806C>G (p.Pro2602=) rs200241260
NM_032119.4(ADGRV1):c.8161A>G (p.Ile2721Val) rs201963060
NM_032119.4(ADGRV1):c.8396C>T (p.Pro2799Leu) rs200179979
NM_032119.4(ADGRV1):c.8572A>G (p.Ile2858Val) rs41308297
NM_032119.4(ADGRV1):c.8651T>C (p.Val2884Ala) rs111033517
NM_032119.4(ADGRV1):c.8730+9_8730+10del rs780180737
NM_032119.4(ADGRV1):c.8815C>T (p.Pro2939Ser) rs202211640
NM_032119.4(ADGRV1):c.8938T>C (p.Leu2980=) rs397517442
NM_032119.4(ADGRV1):c.9083A>G (p.Asn3028Ser) rs150549897
NM_032119.4(ADGRV1):c.9181A>G (p.Ile3061Val) rs759038879
NM_032119.4(ADGRV1):c.9213C>T (p.Asp3071=) rs56329646
NM_032119.4(ADGRV1):c.9447+6G>A rs201481219
NM_032119.4(ADGRV1):c.9466A>G (p.Ile3156Val) rs372484022
NM_032119.4(ADGRV1):c.9496T>G (p.Tyr3166Asp) rs371646432
NM_032119.4(ADGRV1):c.9558C>T (p.Thr3186=) rs201089046
NM_032119.4(ADGRV1):c.9635T>C (p.Ile3212Thr) rs199833843
NM_032119.4(ADGRV1):c.9650C>T (p.Ala3217Val) rs114137750
NM_032119.4(ADGRV1):c.9772G>A (p.Val3258Ile) rs764987437

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.