Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.6779554T>C | CA14826040 | BMP2 | c.*465T>C (n.*465T>C) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.6779554T>G | CA1015119649 | BMP2 | c.*465T>G (n.*465T>G) | dbSNP gnomAD v3 gnomAD v4 |
20 | g.6779554T= | CA2348112563 | BMP2 | c.*465T= (n.*465T=) | dbSNP |