Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.3414616T>C | CA144647 | PRDM16 | c.2660T>C (p.Leu887Pro) c.2084T>C (p.Leu695Pro) c.2663T>C (p.Leu888Pro) n.2438T>C c.2108T>C (p.Leu703Pro) c.2657T>C (p.Leu886Pro) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
1 | g.3414616T= | CA1143526221 | PRDM16 | c.2660T= (p.Leu887=) c.2084T= (p.Leu695=) c.2663T= (p.Leu888=) n.2438T= c.2108T= (p.Leu703=) c.2657T= (p.Leu886=) | dbSNP |