ClinVar Miner

List of variants in gene FAT2 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 85
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001447.3(FAT2):c.742C>T (p.Pro248Ser) rs3734061 0.00579
NM_001447.3(FAT2):c.829G>C (p.Val277Leu) rs145834206 0.00429
NM_001447.3(FAT2):c.3399C>A (p.Asn1133Lys) rs138913417 0.00132
NM_001447.3(FAT2):c.3555T>C (p.Phe1185=) rs116378153 0.00064
NM_001447.3(FAT2):c.214C>T (p.Arg72Trp) rs147574119 0.00013
NM_001447.3(FAT2):c.2868C>T (p.Pro956=) rs374807522 0.00004
NM_001447.3(FAT2):c.1018G>A (p.Gly340Ser)
NM_001447.3(FAT2):c.1047C>T (p.Gly349=)
NM_001447.3(FAT2):c.1086C>G (p.Phe362Leu)
NM_001447.3(FAT2):c.1110G>A (p.Gln370=)
NM_001447.3(FAT2):c.1140C>T (p.Arg380=)
NM_001447.3(FAT2):c.1185T>C (p.Tyr395=)
NM_001447.3(FAT2):c.1211T>A (p.Val404Glu)
NM_001447.3(FAT2):c.1277G>A (p.Arg426Lys)
NM_001447.3(FAT2):c.1311G>A (p.Pro437=)
NM_001447.3(FAT2):c.1326C>T (p.Thr442=)
NM_001447.3(FAT2):c.1341C>T (p.Asp447=)
NM_001447.3(FAT2):c.1398C>T (p.Thr466=)
NM_001447.3(FAT2):c.13C>G (p.Leu5Val)
NM_001447.3(FAT2):c.1473A>G (p.Gly491=)
NM_001447.3(FAT2):c.1518T>C (p.Ser506=)
NM_001447.3(FAT2):c.153T>C (p.Tyr51=)
NM_001447.3(FAT2):c.1677C>T (p.Asp559=)
NM_001447.3(FAT2):c.1710A>G (p.Thr570=)
NM_001447.3(FAT2):c.1746G>A (p.Ser582=)
NM_001447.3(FAT2):c.1750A>T (p.Met584Leu)
NM_001447.3(FAT2):c.1821A>G (p.Leu607=)
NM_001447.3(FAT2):c.1863C>T (p.Leu621=)
NM_001447.3(FAT2):c.1880A>G (p.Asn627Ser)
NM_001447.3(FAT2):c.2049C>T (p.Ile683=)
NM_001447.3(FAT2):c.2059A>G (p.Ile687Val)
NM_001447.3(FAT2):c.2088T>C (p.Asp696=)
NM_001447.3(FAT2):c.2112A>G (p.Thr704=)
NM_001447.3(FAT2):c.2151C>T (p.His717=)
NM_001447.3(FAT2):c.2165T>C (p.Ile722Thr)
NM_001447.3(FAT2):c.2196C>T (p.Thr732=)
NM_001447.3(FAT2):c.2263G>T (p.Ala755Ser)
NM_001447.3(FAT2):c.2310G>A (p.Gly770=)
NM_001447.3(FAT2):c.2436C>T (p.Asp812=) rs762885613
NM_001447.3(FAT2):c.2448C>T (p.Asn816=)
NM_001447.3(FAT2):c.2496C>T (p.Asp832=)
NM_001447.3(FAT2):c.2497A>G (p.Thr833Ala)
NM_001447.3(FAT2):c.2556T>C (p.Asn852=)
NM_001447.3(FAT2):c.2571C>T (p.Tyr857=)
NM_001447.3(FAT2):c.2601C>T (p.Ser867=)
NM_001447.3(FAT2):c.2649C>T (p.Arg883=)
NM_001447.3(FAT2):c.2663G>A (p.Arg888Gln)
NM_001447.3(FAT2):c.269G>A (p.Gly90Asp)
NM_001447.3(FAT2):c.2841G>A (p.Leu947=)
NM_001447.3(FAT2):c.2940G>C (p.Ala980=)
NM_001447.3(FAT2):c.2943C>T (p.Leu981=)
NM_001447.3(FAT2):c.3022C>T (p.Leu1008=)
NM_001447.3(FAT2):c.3028C>T (p.Arg1010Cys)
NM_001447.3(FAT2):c.3045T>C (p.His1015=)
NM_001447.3(FAT2):c.3057C>T (p.Ile1019=)
NM_001447.3(FAT2):c.319C>T (p.Leu107=)
NM_001447.3(FAT2):c.321G>A (p.Leu107=)
NM_001447.3(FAT2):c.3228A>G (p.Gly1076=)
NM_001447.3(FAT2):c.3296T>C (p.Phe1099Ser)
NM_001447.3(FAT2):c.3300A>G (p.Ala1100=)
NM_001447.3(FAT2):c.3322T>C (p.Leu1108=)
NM_001447.3(FAT2):c.3354T>C (p.Ser1118=)
NM_001447.3(FAT2):c.3363T>G (p.Thr1121=)
NM_001447.3(FAT2):c.3383C>T (p.Thr1128Met)
NM_001447.3(FAT2):c.3384G>A (p.Thr1128=)
NM_001447.3(FAT2):c.3384G>T (p.Thr1128=)
NM_001447.3(FAT2):c.3453C>T (p.Pro1151=)
NM_001447.3(FAT2):c.3465T>G (p.Ser1155=)
NM_001447.3(FAT2):c.3468G>T (p.Val1156=)
NM_001447.3(FAT2):c.3475C>A (p.Leu1159Met)
NM_001447.3(FAT2):c.438T>C (p.Pro146=)
NM_001447.3(FAT2):c.455C>T (p.Ser152Leu)
NM_001447.3(FAT2):c.456G>A (p.Ser152=)
NM_001447.3(FAT2):c.516C>T (p.Ala172=)
NM_001447.3(FAT2):c.555T>C (p.Tyr185=)
NM_001447.3(FAT2):c.567A>C (p.Thr189=)
NM_001447.3(FAT2):c.570G>A (p.Arg190=)
NM_001447.3(FAT2):c.57G>A (p.Glu19=)
NM_001447.3(FAT2):c.594C>G (p.Pro198=)
NM_001447.3(FAT2):c.602G>C (p.Gly201Ala)
NM_001447.3(FAT2):c.621G>T (p.Gly207=)
NM_001447.3(FAT2):c.630C>T (p.Asn210=)
NM_001447.3(FAT2):c.645A>G (p.Gly215=)
NM_001447.3(FAT2):c.675C>A (p.Asp225Glu)
NM_001447.3(FAT2):c.847G>A (p.Gly283Arg)

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.