Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.35657968G>T | CA464450950 | RMRP | n.51C>A | ClinVar dbSNP gnomAD v4 |
9 | g.35657968G>C | CA464450955 | RMRP | n.51C>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.35657968G>A | CA16618856 | RMRP | n.51C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.35657968G= | CA1846127614 | RMRP | n.51C= | dbSNP |