| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC130063398, SNAPC2 (A10V) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (A10S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (E17K) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (S58G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (P45T) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (R57P) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (E53D) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (R57G) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (G20A) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (P11S) | Single nucleotide variant (missense variant) | not specified | |
| | LOC130063398, SNAPC2 (R13C) | Single nucleotide variant (missense variant) | not specified | |
Click to view in NCBI Gene