ClinVar Miner

List of variants in gene CYP4V2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 30
Download table as spreadsheet
HGVS dbSNP
NM_207352.4(CYP4V2):c.1269C>T (p.Pro423=)
NM_207352.4(CYP4V2):c.1328G>A (p.Arg443Gln) rs72646291
NM_207352.4(CYP4V2):c.1338C>T (p.Pro446=)
NM_207352.4(CYP4V2):c.1371C>T (p.Tyr457=)
NM_207352.4(CYP4V2):c.1431A>G (p.Glu477=)
NM_207352.4(CYP4V2):c.1434G>A (p.Lys478=)
NM_207352.4(CYP4V2):c.147C>G (p.Pro49=)
NM_207352.4(CYP4V2):c.1563T>C (p.Asn521=) rs770469863
NM_207352.4(CYP4V2):c.168C>G (p.Ala56=)
NM_207352.4(CYP4V2):c.174A>G (p.Pro58=)
NM_207352.4(CYP4V2):c.214+10G>C
NM_207352.4(CYP4V2):c.214+9C>T
NM_207352.4(CYP4V2):c.237G>T (p.Glu79Asp) rs199476185
NM_207352.4(CYP4V2):c.240C>T (p.Tyr80=)
NM_207352.4(CYP4V2):c.264G>A (p.Pro88=)
NM_207352.4(CYP4V2):c.264G>T (p.Pro88=) rs201610304
NM_207352.4(CYP4V2):c.270G>A (p.Leu90=) rs192920673
NM_207352.4(CYP4V2):c.282C>T (p.Val94=) rs142775374
NM_207352.4(CYP4V2):c.327+7A>G
NM_207352.4(CYP4V2):c.367A>G (p.Met123Val) rs149684063
NM_207352.4(CYP4V2):c.37C>T (p.Leu13=) rs765537555
NM_207352.4(CYP4V2):c.414-17A>C
NM_207352.4(CYP4V2):c.414-7T>C
NM_207352.4(CYP4V2):c.423C>T (p.Asn141=)
NM_207352.4(CYP4V2):c.432C>T (p.Arg144=)
NM_207352.4(CYP4V2):c.610G>A (p.Ala204Thr) rs61745524
NM_207352.4(CYP4V2):c.64C>G (p.Leu22Val) rs1055138
NM_207352.4(CYP4V2):c.736C>G (p.Leu246Val) rs531538384
NM_207352.4(CYP4V2):c.988-20A>G
NM_207352.4(CYP4V2):c.988-9C>T

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.