ClinVar Miner

List of variants in gene FGD4 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001370298.3(FGD4):c.*4454G>A rs147515673 0.01373
NM_001370298.3(FGD4):c.1971C>T (p.Ile657=) rs61748364 0.00526
NM_001370298.3(FGD4):c.*2487C>A rs188600194 0.00503
NM_001370298.3(FGD4):c.1777C>A (p.Pro593Thr) rs138160928 0.00168
NM_001370298.3(FGD4):c.666A>T (p.Ala222=) rs139357821 0.00161
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met) rs61753359 0.00131
NM_001370298.3(FGD4):c.167-29728T>C rs561223009 0.00065
NM_001370298.3(FGD4):c.890G>A (p.Gly297Asp) rs201826412 0.00024
NM_001370298.3(FGD4):c.1923-7A>G rs200542541 0.00021
NM_001370298.3(FGD4):c.1973A>G (p.Asp658Gly) rs141237776 0.00015
NM_001370298.3(FGD4):c.2132C>T (p.Ala711Val) rs1341534652 0.00001
NM_001370298.3(FGD4):c.2616C>T (p.Ile872=) rs759982135 0.00001
NM_001370298.3(FGD4):c.1081C>T (p.Arg361Ter) rs118203972
NM_001370298.3(FGD4):c.1098T>C (p.Asp366=)
NM_001370298.3(FGD4):c.1405-7A>G rs1948890717
NM_001370298.3(FGD4):c.2122C>A (p.Pro708Thr) rs144693221
NM_001370298.3(FGD4):c.2141G>A (p.Arg714Gln) rs372890690
NM_001370298.3(FGD4):c.376C>A (p.Pro126Thr) rs199744649
NM_001370298.3(FGD4):c.875_878del (p.Ser292fs)

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.