Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.153774047G>T | CA415122455 | PLXNB3 | c.3468G>T (p.Glu1156Asp) c.3537G>T (p.Glu1179Asp) | dbSNP gnomAD v4 |
X | g.153774047G>C | CA337235033 | PLXNB3 | c.3468G>C (p.Glu1156Asp) c.3537G>C (p.Glu1179Asp) | dbSNP gnomAD v3 gnomAD v4 |