| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.40799092G>C | CA16619808 | SLC25A15,TPTE2P5 | c.91G>C (p.Asp31His) n.412G>C n.2255C>G n.2084C>G | ClinVar dbSNP COSMIC |
| 13 | g.40799092G>T | CA6959621 | SLC25A15,TPTE2P5 | c.91G>T (p.Asp31Tyr) n.412G>T n.2255C>A n.2084C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.40799092G>A | CA6959622 | SLC25A15,TPTE2P5 | c.91G>A (p.Asp31Asn) n.412G>A n.2255C>T n.2084C>T | dbSNP ExAC gnomAD v2 |
| 13 | g.40799092G= | CA2086588816 | SLC25A15,TPTE2P5 | c.91G= (p.Asp31=) n.412G= n.2255C= n.2084C= | dbSNP |