Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52469683_52469710delinsCCTCCAGCAGCTTGCGGTAGGTGGCGAT | CA2036492909 | KRT6C | c.1384_1411delinsATCGCCACCTACCGCAAGCTGCTGGAGG (p.Ile462=) | |
12 | g.52469689_52469715del | CA151185 | KRT6C | c.1384_1410del (p.Ile462_Glu470del) | ClinVar dbSNP |
12 | g.52469689G>A | CA480068839 | KRT6C | c.1405C>T (p.Leu469=) | |
12 | g.52469689G>C | CA384934638 | KRT6C | c.1405C>G (p.Leu469Val) | |
12 | g.52469689G>T | CA384934641 | KRT6C | c.1405C>A (p.Leu469Met) | COSMIC |
12 | g.52469690C>A | CA480068840 | KRT6C | c.1404G>T (p.Leu468=) | |
12 | g.52469690C= | CA2036492923 | KRT6C | c.1404G= (p.Leu468=) | |
12 | g.52469690C>G | CA480068842 | KRT6C | c.1404G>C (p.Leu468=) | |
12 | g.52469690C>T | CA480068841 | KRT6C | c.1404G>A (p.Leu468=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52469691A>C | CA384934645 | KRT6C | c.1403T>G (p.Leu468Arg) | |
12 | g.52469691A>G | CA384934648 | KRT6C | c.1403T>C (p.Leu468Pro) | |
12 | g.52469691A>T | CA384934649 | KRT6C | c.1403T>A (p.Leu468Gln) | |
12 | g.52469692G>A | CA480068843 | KRT6C | c.1402C>T (p.Leu468=) | |
12 | g.52469692G>C | CA384934651 | KRT6C | c.1402C>G (p.Leu468Val) | |
12 | g.52469692G>T | CA384934650 | KRT6C | c.1402C>A (p.Leu468Met) | |
12 | g.52469693C>A | CA384934653 | KRT6C | c.1401G>T (p.Lys467Asn) | |
12 | g.52469693C= | CA2036492930 | KRT6C | c.1401G= (p.Lys467=) | |
12 | g.52469693C>G | CA384934654 | KRT6C | c.1401G>C (p.Lys467Asn) | |
12 | g.52469693C>T | CA6581136 | KRT6C | c.1401G>A (p.Lys467=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52469694T>A | CA384934662 | KRT6C | c.1400A>T (p.Lys467Met) | |
12 | g.52469694T>C | CA384934666 | KRT6C | c.1400A>G (p.Lys467Arg) | |
12 | g.52469694T>G | CA384934669 | KRT6C | c.1400A>C (p.Lys467Thr) | |
12 | g.52469695T>A | CA6581137 | KRT6C | c.1399A>T (p.Lys467Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52469695T>C | CA384934674 | KRT6C | c.1399A>G (p.Lys467Glu) | |
12 | g.52469695T>G | CA384934675 | KRT6C | c.1399A>C (p.Lys467Gln) | |
12 | g.52469695T= | CA2036492936 | KRT6C | c.1399A= (p.Lys467=) | |
12 | g.52469696G>A | CA480068844 | KRT6C | c.1398C>T (p.Arg466=) | |
12 | g.52469696G>C | CA480068845 | KRT6C | c.1398C>G (p.Arg466=) | |
12 | g.52469696G>T | CA480068846 | KRT6C | c.1398C>A (p.Arg466=) | |
12 | g.52469697C>A | CA384934678 | KRT6C | c.1397G>T (p.Arg466Leu) | gnomAD v4 |
12 | g.52469697C= | CA2036492938 | KRT6C | c.1397G= (p.Arg466=) | |
12 | g.52469697C>G | CA384934679 | KRT6C | c.1397G>C (p.Arg466Pro) | |
12 | g.52469697C>T | CA6581138 | KRT6C | c.1397G>A (p.Arg466His) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52469698G>A | CA6581139 | KRT6C | c.1396C>T (p.Arg466Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
12 | g.52469698G>C | CA384934706 | KRT6C | c.1396C>G (p.Arg466Gly) | |
12 | g.52469698G= | CA2036492943 | KRT6C | c.1396C= (p.Arg466=) | |
12 | g.52469698G>T | CA384934681 | KRT6C | c.1396C>A (p.Arg466Ser) | |
12 | g.52469699G>A | CA480068847 | KRT6C | c.1395C>T (p.Tyr465=) | |
12 | g.52469699G>C | CA384934712 | KRT6C | c.1395C>G (p.Tyr465Ter) | |
12 | g.52469699G>T | CA384934715 | KRT6C | c.1395C>A (p.Tyr465Ter) | gnomAD v4 |
12 | g.52469700T>A | CA384934724 | KRT6C | c.1394A>T (p.Tyr465Phe) | |
12 | g.52469700T>C | CA384934725 | KRT6C | c.1394A>G (p.Tyr465Cys) | gnomAD v4 |
12 | g.52469700T>G | CA384934726 | KRT6C | c.1394A>C (p.Tyr465Ser) | |
12 | g.52469701A>C | CA384934730 | KRT6C | c.1393T>G (p.Tyr465Asp) | |
12 | g.52469701A>G | CA384934727 | KRT6C | c.1393T>C (p.Tyr465His) | |
12 | g.52469701A>T | CA384934728 | KRT6C | c.1393T>A (p.Tyr465Asn) | |
12 | g.52469702G>A | CA480068848 | KRT6C | c.1392C>T (p.Thr464=) | gnomAD v4 |
12 | g.52469702G>C | CA480068850 | KRT6C | c.1392C>G (p.Thr464=) | dbSNP gnomAD v2 gnomAD v4 |
12 | g.52469702G= | CA2036492952 | KRT6C | c.1392C= (p.Thr464=) | |
12 | g.52469702G>T | CA480068849 | KRT6C | c.1392C>A (p.Thr464=) |