Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.72888378C>G | CA347231468 | SPR | c.369C>G (p.Tyr123Ter) n.356-42C>G | ClinVar dbSNP gnomAD v4 |
2 | g.72888378C>T | CA1708942 | SPR | c.369C>T (p.Tyr123=) n.356-42C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.72888378C= | CA1260703850 | SPR | c.369C= (p.Tyr123=) n.356-42C= | dbSNP |