Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.35657756C>T | CA192745529 | RMRP | n.263G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.35657756C>A | CA257181 | RMRP | n.263G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.35657756C>G | CA464450131 | RMRP | n.263G>C | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.35657756C= | CA1846127357 | RMRP | n.263G= | dbSNP |