ClinVar Miner

List of variants in gene FAT4 reported by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 20
Download table as spreadsheet
HGVS dbSNP
NM_001291303.3(FAT4):c.13193T>C (p.Ile4398Thr) rs200729108
NM_001291303.3(FAT4):c.14841T>A (p.Asp4947Glu) rs768693221
NM_001291303.3(FAT4):c.4543G>A (p.Val1515Met)
NM_001291303.3(FAT4):c.5792A>G (p.Tyr1931Cys)
NM_001291303.3(FAT4):c.739C>T (p.Pro247Ser) rs191329848
NM_001291303.3(FAT4):c.7578C>T (p.Ala2526=) rs748125780
NM_001291303.3(FAT4):c.8162A>G (p.Asn2721Ser) rs1452280145
NM_001291303.3(FAT4):c.8280A>C (p.Lys2760Asn) rs750907829
NM_001291303.3(FAT4):c.8290A>C (p.Asn2764His) rs147281598
NM_001291303.3(FAT4):c.8417A>C (p.Asn2806Thr)
NM_024582.4(FAT4):c.10384A>G (p.Ile3462Val) rs147872710
NM_024582.4(FAT4):c.10847C>T (p.Thr3616Met) rs111423173
NM_024582.4(FAT4):c.1128G>A (p.Val376=) rs202216461
NM_024582.4(FAT4):c.13286A>T (p.Asp4429Val) rs774943740
NM_024582.4(FAT4):c.4526G>A (p.Arg1509Gln) rs776836295
NM_024582.4(FAT4):c.524G>T (p.Arg175Leu) rs143534324
NM_024582.4(FAT4):c.5401C>T (p.Arg1801Trp) rs201887525
NM_024582.4(FAT4):c.6977C>T (p.Thr2326Ile) rs200344386
NM_024582.4(FAT4):c.739C>A (p.Pro247Thr) rs191329848
NM_024582.4(FAT4):c.9150C>A (p.Asp3050Glu) rs761372826

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.