Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.174729165T>A | CA3565194 | MSX2 | c.386T>A (p.Met129Lys) c.*10T>A (n.*10T>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.174729165T>C | CA3565193 | MSX2 | c.386T>C (p.Met129Thr) c.*10T>C (n.*10T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.174729165T>G | CA3565195 | MSX2 | c.386T>G (p.Met129Arg) c.*10T>G (n.*10T>G) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |