Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
13 | g.77920970A>C | CA2103834434 | EDNRB | c.-51-2346T>G (n.-51-2346T>G) | dbSNP |
13 | g.77920970A>G | CA15778659 | EDNRB | c.-51-2346T>C (n.-51-2346T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
13 | g.77920970A= | CA2103834433 | EDNRB | c.-51-2346T= (n.-51-2346T=) | dbSNP |