ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 27
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 12p11.21(chr12:32608165-32825558)x1
GRCh37/hg19 12p11.21(chr12:32616797-32713135)x1
NM_001304481.1(FGD4):c.220C>A (p.Pro74Thr) rs199744649
NM_001370298.3(FGD4):c.1769A>C (p.Tyr590Ser)
NM_001370298.3(FGD4):c.1961A>G (p.Gln654Arg)
NM_001370298.3(FGD4):c.2509C>A (p.Pro837Thr)
NM_001370298.3(FGD4):c.2602T>C (p.Trp868Arg)
NM_139241.3(FGD4):c.-245-29728T>C rs561223009
NM_139241.3(FGD4):c.1097T>C (p.Leu366Ser) rs555510533
NM_139241.3(FGD4):c.1203G>C (p.Lys401Asn) rs1131691394
NM_139241.3(FGD4):c.1278A>C (p.Glu426Asp) rs879254000
NM_139241.3(FGD4):c.1366C>A (p.Pro456Thr) rs138160928
NM_139241.3(FGD4):c.1562A>G (p.Asp521Gly) rs141237776
NM_139241.3(FGD4):c.1711C>G (p.Pro571Ala) rs144693221
NM_139241.3(FGD4):c.1712C>A (p.Pro571His) rs145071617
NM_139241.3(FGD4):c.1721C>T (p.Ala574Val) rs1341534652
NM_139241.3(FGD4):c.1878A>C (p.Glu626Asp)
NM_139241.3(FGD4):c.2149G>A (p.Val717Met) rs61753359
NM_139241.3(FGD4):c.329T>C (p.Leu110Pro) rs142609007
NM_139241.3(FGD4):c.381A>G (p.Ile127Met) rs774466701
NM_139241.3(FGD4):c.479G>A (p.Gly160Asp) rs201826412
NM_139241.3(FGD4):c.484G>C (p.Gly162Arg) rs774679169
NM_139241.3(FGD4):c.50C>G (p.Pro17Arg) rs371407163
NM_139241.3(FGD4):c.569T>A (p.Leu190Gln) rs144980336
NM_139241.3(FGD4):c.597G>C (p.Met199Ile) rs1592295526
NM_139241.3(FGD4):c.955C>T (p.Arg319Cys) rs1131691854
NM_139241.3(FGD4):c.994-7A>G

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.