Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
X | g.137030751C>T | CA10529119 | GPR101,TM9SF5P | n.358-29774C>T c.924G>A (p.Glu308=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.137030751C>G | CA180516 | GPR101,TM9SF5P | n.358-29774C>G c.924G>C (p.Glu308Asp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |