| | LOC126807255, FAT1 (S2941R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (E4558K) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (P4536R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (P4495L) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (N4492S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (N4492H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (S4386P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (I3730M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (V3634I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (A3518T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (I3627F) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | | Single nucleotide variant (synonymous variant) | FAT1-related condition | |
| | | Single nucleotide variant (intron variant) | FAT1-related condition | |
| | | Single nucleotide variant (synonymous variant) | FAT1-related condition | |
| | | Single nucleotide variant (3 prime UTR variant) | FAT1-related condition | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | FAT1-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | FAT1-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807254 (R3665*) | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | FAT1-related condition +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807253 (I4397V) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807255 (A2889V) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (R3668W) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807253 (T4543A) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807254 (D3583N) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC132090718 (K1623E) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807255 (I2937V) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807254 (V3616I) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807255 (K2886N) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807253 (S4566N) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807255 (R2917*) | Single nucleotide variant (nonsense) | FAT1-related condition | |
| | FAT1, LOC126807254 (R3668L) | Single nucleotide variant (missense variant) | FAT1-related condition | |
| | FAT1, LOC126807253 (A4529V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (I2950T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (V2887A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (A4471V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (T2909P) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (Q4502R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (A2833V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (D3749E) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807255 (T2997S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (A4544T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (T3720S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (A4471T) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (P2823L) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FAT1, LOC126807253 (V4549M) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FAT1, LOC126807253 (L4451F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (P4426S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (P2813S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (Y4403C) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (R3661H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (Q3679R) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (L2872S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (P2963A) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (R4513G) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (P4395L) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FAT1, LOC126807255 (D2905E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (V4532I) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (D4497N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (A4419T) | Single nucleotide variant (missense variant) | Inborn genetic diseases +1 more | GConflicting classifications of pathogenicity |
| | FAT1, LOC126807254 (I3533V) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (N2863S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807254 (Y3580H) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807255 (T2943M) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | FAT1, LOC126807253 (T4422M) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807255 (K2886E) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126807255, FAT1 (R2917Q) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807254 (S3554A) | Indel (missense variant) | not provided | |
| | FAT1, LOC126807255 (A2968G) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (V3694I) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (I3722T) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (R3674S) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807254 (P3688L) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (S3555F) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807255 (S2812I) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126807255, FAT1 (F2860S) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807253 (C4553R) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807253 (V4559I) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | FAT1, LOC126807255 (G2825R) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (R3773H) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | FAT1, LOC126807254 (L3696P) | Single nucleotide variant (missense variant) | not provided | |
| | FAT1, LOC126807254 (D3626N) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |