Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.127421397A>C | CA114402 | PROC | c.185A>C (p.Glu62Ala) c.150A>C (p.Gly50=) n.268A>C c.368A>C (p.Glu123Ala) c.248A>C (p.Glu83Ala) c.428A>C (p.Glu143Ala) c.269A>C (p.Glu90Ala) c.161A>C (p.Glu54Ala) c.179A>C (p.Glu60Ala) | ClinVar dbSNP |
2 | g.127421397A= | CA1286880887 | PROC | c.185A= (p.Glu62=) c.150A= (p.Gly50=) n.268A= c.368A= (p.Glu123=) c.248A= (p.Glu83=) c.428A= (p.Glu143=) c.269A= (p.Glu90=) c.161A= (p.Glu54=) c.179A= (p.Glu60=) | dbSNP |