Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.52452153G>A | CA353168551 | TNNC1 | c.155C>T (p.Pro52Leu) c.23C>T (p.Pro8Leu) | ClinVar dbSNP |
3 | g.52452153G>C | CA297343 | TNNC1 | c.155C>G (p.Pro52Arg) c.23C>G (p.Pro8Arg) | ClinVar dbSNP |
3 | g.52452153G= | CA1364863982 | TNNC1 | c.155C= (p.Pro52=) c.23C= (p.Pro8=) | dbSNP |