| | TTC3, TTC3-AS1 (T1017K +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (P1105A +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (P1065R +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (R1818Q +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (N1863S +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | TTC3, TTC3-AS1 (S1385F +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (G1831R +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | TTC3, TTC3-AS1 (S1737F +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | TTC3, TTC3-AS1 (S1669N +4 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not specified | |
| | LOC125418073, TTC3 (L1446F +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | TTC3, TTC3-AS1 (I1712S +4 more) | Single nucleotide variant (missense variant) | not specified | |
| | LOC125418073, TTC3 (V1543M +4 more) | Single nucleotide variant (missense variant) | Corticobasal syndrome | |
| | TTC3, TTC3-AS1 (A943G +4 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | LOC125418073, TTC3 (R1522C +4 more) | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | LOC125418073, TTC3 (E1021K +4 more) | Single nucleotide variant (missense variant) | not provided | |