Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.93586312T>A | CA242005064 | SOCS2 | c.591+11139T>A (n.591+11139T>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.93586312T>C | CA2055419746 | SOCS2 | c.591+11139T>C (n.591+11139T>C) | dbSNP |
12 | g.93586312T= | CA2055419744 | SOCS2 | c.591+11139T= (n.591+11139T=) | dbSNP |
12 | g.93586312T>G | CA2844609355 | SOCS2 | c.591+11139T>G (n.591+11139T>G) | dbSNP |