ClinVar Miner

List of variants in gene CYP4V2 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 123
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_207352.4(CYP4V2):c.327+11G>C rs62350517 0.05079
NM_207352.4(CYP4V2):c.823G>A (p.Glu275Lys) rs34745240 0.03921
NM_207352.4(CYP4V2):c.638G>A (p.Ser213Asn) rs34331648 0.02714
NM_207352.4(CYP4V2):c.1091-4T>A rs61748269 0.01211
NM_207352.4(CYP4V2):c.1536C>T (p.Gly512=) rs72646298 0.01209
NM_207352.4(CYP4V2):c.*4T>C rs76978024 0.00479
NM_207352.4(CYP4V2):c.1328G>A (p.Arg443Gln) rs72646291 0.00306
NM_207352.4(CYP4V2):c.610G>A (p.Ala204Thr) rs61745524 0.00299
NM_207352.4(CYP4V2):c.99G>A (p.Leu33=) rs145611966 0.00169
NM_207352.4(CYP4V2):c.1446G>A (p.Ser482=) rs141950964 0.00089
NM_207352.4(CYP4V2):c.270G>A (p.Leu90=) rs192920673 0.00044
NM_207352.4(CYP4V2):c.1493A>C (p.Glu498Ala) rs142244984 0.00035
NM_207352.4(CYP4V2):c.282C>T (p.Val94=) rs142775374 0.00035
NM_207352.4(CYP4V2):c.168C>G (p.Ala56=) rs369484576 0.00024
NM_207352.4(CYP4V2):c.367A>G (p.Met123Val) rs149684063 0.00021
NM_207352.4(CYP4V2):c.240C>T (p.Tyr80=) rs138173968 0.00020
NM_207352.4(CYP4V2):c.674+14T>C rs201205689 0.00020
NM_207352.4(CYP4V2):c.183C>G (p.Gly61=) rs200327267 0.00014
NM_207352.4(CYP4V2):c.214+17C>T rs369891403 0.00012
NM_207352.4(CYP4V2):c.215-6C>T rs372144743 0.00010
NM_207352.4(CYP4V2):c.604+15T>G rs376981886 0.00009
NM_207352.4(CYP4V2):c.414-17A>C rs769815150 0.00008
NM_207352.4(CYP4V2):c.1225+15C>T rs918111674 0.00006
NM_207352.4(CYP4V2):c.414-7T>C rs376204847 0.00005
NM_207352.4(CYP4V2):c.1308C>T (p.Pro436=) rs139324591 0.00004
NM_207352.4(CYP4V2):c.1314G>A (p.Glu438=) rs568563828 0.00004
NM_207352.4(CYP4V2):c.237G>T (p.Glu79Asp) rs199476185 0.00004
NM_207352.4(CYP4V2):c.327+20A>T rs911209750 0.00004
NM_207352.4(CYP4V2):c.1515G>A (p.Leu505=) rs780681619 0.00003
NM_207352.4(CYP4V2):c.214+10G>C rs906756906 0.00003
NM_207352.4(CYP4V2):c.264G>T (p.Pro88=) rs201610304 0.00003
NM_207352.4(CYP4V2):c.1257C>T (p.Ala419=) rs773317651 0.00002
NM_207352.4(CYP4V2):c.1269C>T (p.Pro423=) rs905837185 0.00002
NM_207352.4(CYP4V2):c.1344T>C (p.Asn448=) rs72646292 0.00002
NM_207352.4(CYP4V2):c.1371C>T (p.Tyr457=) rs377057366 0.00002
NM_207352.4(CYP4V2):c.393T>C (p.Leu131=) rs1192960841 0.00002
NM_207352.4(CYP4V2):c.594T>C (p.Asp198=) rs780963135 0.00002
NM_207352.4(CYP4V2):c.91C>T (p.Leu31=) rs1006582614 0.00002
NM_207352.4(CYP4V2):c.120C>T (p.Tyr40=) rs1481160549 0.00001
NM_207352.4(CYP4V2):c.1290G>A (p.Pro430=) rs113521707 0.00001
NM_207352.4(CYP4V2):c.1362A>G (p.Pro454=) rs1038955378 0.00001
NM_207352.4(CYP4V2):c.1431A>G (p.Glu477=) rs545708982 0.00001
NM_207352.4(CYP4V2):c.147C>G (p.Pro49=) rs769901483 0.00001
NM_207352.4(CYP4V2):c.1527A>G (p.Pro509=) rs527378526 0.00001
NM_207352.4(CYP4V2):c.1557G>A (p.Arg519=) rs200291603 0.00001
NM_207352.4(CYP4V2):c.1563T>C (p.Asn521=) rs770469863 0.00001
NM_207352.4(CYP4V2):c.327+7A>G rs1736092378 0.00001
NM_207352.4(CYP4V2):c.348G>A (p.Lys116=) rs778488831 0.00001
NM_207352.4(CYP4V2):c.408T>G (p.Leu136=) rs761616967 0.00001
NM_207352.4(CYP4V2):c.413+20T>C rs1463691611 0.00001
NM_207352.4(CYP4V2):c.423C>T (p.Asn141=) rs370950185 0.00001
NM_207352.4(CYP4V2):c.736C>G (p.Leu246Val) rs531538384 0.00001
NM_207352.4(CYP4V2):c.780C>G (p.Ile260Met) rs753561422 0.00001
NM_207352.4(CYP4V2):c.802-14T>C rs1415799555 0.00001
NM_207352.4(CYP4V2):c.831C>T (p.Asn277=) rs72646276 0.00001
NM_207352.4(CYP4V2):c.903C>T (p.Asp301=) rs759445878 0.00001
NM_207352.4(CYP4V2):c.988-20A>G rs781744552 0.00001
NM_207352.4(CYP4V2):c.*210dup rs199938898
NM_207352.4(CYP4V2):c.1008T>C (p.Ala336=)
NM_207352.4(CYP4V2):c.1011A>G (p.Ala337=) rs988098401
NM_207352.4(CYP4V2):c.1090+15T>G rs2126595634
NM_207352.4(CYP4V2):c.1091-11G>C
NM_207352.4(CYP4V2):c.1091-15A>G rs1300763823
NM_207352.4(CYP4V2):c.1091-20T>G rs773179019
NM_207352.4(CYP4V2):c.1101C>T (p.Asp367=)
NM_207352.4(CYP4V2):c.1107C>T (p.Pro369=)
NM_207352.4(CYP4V2):c.1152T>C (p.Val384=)
NM_207352.4(CYP4V2):c.1197C>G (p.Ala399=) rs1304200174
NM_207352.4(CYP4V2):c.1197C>T (p.Ala399=) rs1304200174
NM_207352.4(CYP4V2):c.1215T>C (p.Asp405=)
NM_207352.4(CYP4V2):c.1225+10C>T
NM_207352.4(CYP4V2):c.1225+20A>G rs2126600924
NM_207352.4(CYP4V2):c.1225+9G>A
NM_207352.4(CYP4V2):c.1226-13T>C
NM_207352.4(CYP4V2):c.1226-16G>T rs1379961249
NM_207352.4(CYP4V2):c.1226-7T>C
NM_207352.4(CYP4V2):c.1272T>C (p.Tyr424=) rs2126601269
NM_207352.4(CYP4V2):c.1338C>G (p.Pro446=) rs35524919
NM_207352.4(CYP4V2):c.1338C>T (p.Pro446=) rs35524919
NM_207352.4(CYP4V2):c.1368C>T (p.Ala456=) rs2126601567
NM_207352.4(CYP4V2):c.1377C>T (p.Pro459=)
NM_207352.4(CYP4V2):c.1405+9C>A
NM_207352.4(CYP4V2):c.1434G>A (p.Lys478=) rs2126603520
NM_207352.4(CYP4V2):c.1446G>C (p.Ser482=)
NM_207352.4(CYP4V2):c.1446G>T (p.Ser482=)
NM_207352.4(CYP4V2):c.1479C>T (p.Asn493=) rs374270799
NM_207352.4(CYP4V2):c.1513T>C (p.Leu505=)
NM_207352.4(CYP4V2):c.174A>G (p.Pro58=) rs763590093
NM_207352.4(CYP4V2):c.175C>T (p.Leu59=)
NM_207352.4(CYP4V2):c.189G>A (p.Ala63=) rs1194791521
NM_207352.4(CYP4V2):c.214+12C>T
NM_207352.4(CYP4V2):c.214+7G>A
NM_207352.4(CYP4V2):c.214+9C>A
NM_207352.4(CYP4V2):c.214+9C>G
NM_207352.4(CYP4V2):c.214+9C>T rs768506789
NM_207352.4(CYP4V2):c.215-20A>T rs762316724
NM_207352.4(CYP4V2):c.231C>A (p.Ile77=)
NM_207352.4(CYP4V2):c.234T>C (p.Ile78=)
NM_207352.4(CYP4V2):c.258C>T (p.His86=)
NM_207352.4(CYP4V2):c.264G>A (p.Pro88=) rs201610304
NM_207352.4(CYP4V2):c.306T>C (p.Leu102=)
NM_207352.4(CYP4V2):c.345A>G (p.Ser115=) rs2126583809
NM_207352.4(CYP4V2):c.413+10T>C rs750267362
NM_207352.4(CYP4V2):c.413+7del
NM_207352.4(CYP4V2):c.413+8A>C
NM_207352.4(CYP4V2):c.414-13A>T
NM_207352.4(CYP4V2):c.426A>G (p.Lys142=) rs1274455104
NM_207352.4(CYP4V2):c.432C>T (p.Arg144=) rs2126584790
NM_207352.4(CYP4V2):c.597C>T (p.Ile199=) rs2126585104
NM_207352.4(CYP4V2):c.604+12C>T
NM_207352.4(CYP4V2):c.605-13C>T
NM_207352.4(CYP4V2):c.605-4A>G
NM_207352.4(CYP4V2):c.675-8A>G rs2126587113
NM_207352.4(CYP4V2):c.717T>G (p.Leu239=)
NM_207352.4(CYP4V2):c.801+19C>A
NM_207352.4(CYP4V2):c.802-18A>G
NM_207352.4(CYP4V2):c.936C>T (p.Asn312=)
NM_207352.4(CYP4V2):c.969T>C (p.Val323=) rs755534356
NM_207352.4(CYP4V2):c.987+14T>A
NM_207352.4(CYP4V2):c.988-12C>T
NM_207352.4(CYP4V2):c.988-19T>C
NM_207352.4(CYP4V2):c.988-9C>T rs1391055809
NM_207352.4(CYP4V2):c.993C>T (p.His331=)

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.