ClinVar Miner

List of variants in gene FRMPD4 reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001368397.1(FRMPD4):c.741C>G (p.Leu247=) rs7049642 0.01254
NM_001368397.1(FRMPD4):c.3899C>A (p.Thr1300Asn) rs139367112 0.00175
NM_001368397.1(FRMPD4):c.3822C>G (p.Thr1274=) rs140304936 0.00108
NM_001368397.1(FRMPD4):c.1218G>A (p.Lys406=) rs140428359 0.00048
NM_001368397.1(FRMPD4):c.3438A>C (p.Gln1146His) rs139151624 0.00042
NM_001368397.1(FRMPD4):c.2878G>A (p.Ala960Thr) rs138299368 0.00039
NM_001368397.1(FRMPD4):c.1398C>T (p.His466=) rs201869535 0.00033
NM_001368397.1(FRMPD4):c.2599A>G (p.Asn867Asp) rs144170600 0.00023
NM_001368397.1(FRMPD4):c.1736C>T (p.Thr579Met) rs149409320 0.00020
NM_001368397.1(FRMPD4):c.2072G>T (p.Gly691Val) rs200183778 0.00019
NM_001368397.1(FRMPD4):c.1452C>G (p.Leu484=) rs372073451 0.00017
NM_001368397.1(FRMPD4):c.1021G>A (p.Ala341Thr) rs142194011 0.00016
NM_001368397.1(FRMPD4):c.1411G>A (p.Glu471Lys) rs747574742 0.00009
NM_001368397.1(FRMPD4):c.1840G>A (p.Gly614Arg) rs748144907 0.00007
NM_001368397.1(FRMPD4):c.2280C>T (p.Leu760=) rs780060901 0.00007
NM_001368397.1(FRMPD4):c.1896C>A (p.Thr632=) rs369092267 0.00005
NM_001368397.1(FRMPD4):c.2820C>T (p.His940=) rs765472737 0.00005
NM_001368397.1(FRMPD4):c.2605G>A (p.Val869Ile) rs146534723 0.00004
NM_001368397.1(FRMPD4):c.437C>T (p.Ser146Leu) rs2059881267 0.00004
NM_001368397.1(FRMPD4):c.125C>T (p.Thr42Met) rs146122430 0.00001
NM_001368397.1(FRMPD4):c.1926A>G (p.Ala642=) rs887954550 0.00001
NM_001368397.1(FRMPD4):c.2183C>T (p.Ala728Val) rs1294169574 0.00001
NM_001368397.1(FRMPD4):c.249G>A (p.Arg83=) rs761069076 0.00001
NM_001368397.1(FRMPD4):c.3466T>C (p.Cys1156Arg) rs1430635493 0.00001
NM_001368397.1(FRMPD4):c.42-9C>A rs765633648 0.00001
NM_001368397.1(FRMPD4):c.1304C>T (p.Ser435Leu) rs750004207
NM_001368397.1(FRMPD4):c.1883G>C (p.Arg628Pro) rs775576730
NM_001368397.1(FRMPD4):c.2184G>A (p.Ala728=)
NM_001368397.1(FRMPD4):c.2812G>T (p.Ala938Ser) rs771844799
NM_001368397.1(FRMPD4):c.2956T>C (p.Ser986Pro) rs2519858875
NM_001368397.1(FRMPD4):c.424A>G (p.Ser142Gly) rs2519724179

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.