Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.14141665C>T | CA024568 | TMEM43 | c.*1103C>T (n.*1103C>T) c.1073C>T (p.Ser358Leu) n.327+2368C>T c.236+2368C>T c.968C>T (p.Ser323Leu) | ClinVar dbSNP gnomAD v4 COSMIC |
3 | g.14141665C= | CA1346973844 | TMEM43 | c.*1103C= (n.*1103C=) c.1073C= (p.Ser358=) n.327+2368C= c.236+2368C= c.968C= (p.Ser323=) | dbSNP |