List of variants in gene FAT4 reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_001291303.3(FAT4):c.2811G>T (p.Lys937Asn)	rs112454576	0.00367
NM_001291303.3(FAT4):c.12070C>T (p.Arg4024Trp)	rs138019311	0.00333
NM_001291303.3(FAT4):c.5987A>G (p.Lys1996Arg)	rs140055438	0.00242
NM_001291303.3(FAT4):c.5275A>G (p.Ile1759Val)	rs145639192	0.00135
NM_001291303.3(FAT4):c.3424G>A (p.Val1142Met)	rs202188213	0.00127
NM_001291303.3(FAT4):c.3682C>G (p.Gln1228Glu)	rs200227715	0.00086
NM_001291303.3(FAT4):c.7231A>T (p.Thr2411Ser)	rs147297895	0.00084
NM_001291303.3(FAT4):c.13417G>A (p.Val4473Ile)	rs145835705	0.00048
NM_001291303.3(FAT4):c.9602A>G (p.Tyr3201Cys)	rs115895451	0.00042
NM_001291303.3(FAT4):c.8078C>T (p.Ser2693Leu)	rs148918820	0.00025
NM_001291303.3(FAT4):c.11378T>C (p.Leu3793Pro)	rs149757393	0.00023
NM_001291303.3(FAT4):c.6970C>T (p.Arg2324Trp)	rs559079176	0.00014
NM_001291303.3(FAT4):c.7813A>G (p.Ile2605Val)	rs745697037	0.00009
NM_001291303.3(FAT4):c.9964G>A (p.Val3322Met)	rs181641041	0.00008
NM_001291303.3(FAT4):c.9597T>A (p.Asp3199Glu)	rs568003396	0.00005
NM_001291303.3(FAT4):c.14311C>T (p.Arg4771Cys)	rs144845192	0.00004
NM_001291303.3(FAT4):c.3328G>A (p.Glu1110Lys)	rs377275274	0.00004
NM_001291303.3(FAT4):c.11482G>A (p.Val3828Ile)	rs773534151	0.00003
NM_001291303.3(FAT4):c.10940A>G (p.Asp3647Gly)	rs780015426	0.00002
NM_001291303.3(FAT4):c.1163C>T (p.Pro388Leu)	rs991371776	0.00002
NM_001291303.3(FAT4):c.9156C>A (p.Asp3052Glu)	rs761372826	0.00002
NM_001291303.3(FAT4):c.9800A>G (p.His3267Arg)	rs773545119	0.00002
NM_001291303.3(FAT4):c.12017C>T (p.Thr4006Met)	rs776319087	0.00001
NM_001291303.3(FAT4):c.14726C>T (p.Ala4909Val)	rs373253210	0.00001
NM_001291303.3(FAT4):c.5420G>A (p.Arg1807His)	rs768575123	0.00001
NM_001291303.3(FAT4):c.7848T>G (p.Ile2616Met)	rs766719947	0.00001
NM_001291303.3(FAT4):c.8332A>C (p.Ile2778Leu)	rs773858750	0.00001
NM_001291303.3(FAT4):c.9583G>A (p.Val3195Ile)	rs143764643	0.00001
NM_001291303.3(FAT4):c.4726A>C (p.Ile1576Leu)	rs369950066
NM_001291303.3(FAT4):c.7267G>A (p.Ala2423Thr)	rs776977766

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