Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.52447788C>A | CA384981741 | KRT6B | c.1414G>T (p.Glu472Ter) | |
12 | g.52447788C= | CA2036493981 | KRT6B | c.1414G= (p.Glu472=) | |
12 | g.52447788C>G | CA384981745 | KRT6B | c.1414G>C (p.Glu472Gln) | |
12 | g.52447788C>T | CA210845 | KRT6B | c.1414G>A (p.Glu472Lys) | ClinVar dbSNP COSMIC |
12 | g.52447789G>A | CA6580421 | KRT6B | c.1413C>T (p.Gly471=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
12 | g.52447789G>C | CA480068862 | KRT6B | c.1413C>G (p.Gly471=) | |
12 | g.52447789G= | CA2036493990 | KRT6B | c.1413C= (p.Gly471=) | |
12 | g.52447789G>T | CA480068863 | KRT6B | c.1413C>A (p.Gly471=) | |
12 | g.52447790C>A | CA384981758 | KRT6B | c.1412G>T (p.Gly471Val) | |
12 | g.52447790C= | CA2036494001 | KRT6B | c.1412G= (p.Gly471=) | |
12 | g.52447790C>G | CA384981755 | KRT6B | c.1412G>C (p.Gly471Ala) | |
12 | g.52447790C>T | CA384981753 | KRT6B | c.1412G>A (p.Gly471Asp) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.52447791C>A | CA6580422 | KRT6B | c.1411G>T (p.Gly471Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.52447791C= | CA2036494007 | KRT6B | c.1411G= (p.Gly471=) | |
12 | g.52447791C>G | CA384981761 | KRT6B | c.1411G>C (p.Gly471Arg) | |
12 | g.52447791C>T | CA384981763 | KRT6B | c.1411G>A (p.Gly471Ser) | |
12 | g.52447792C>A | CA384981766 | KRT6B | c.1410G>T (p.Glu470Asp) | |
12 | g.52447792C>G | CA384981767 | KRT6B | c.1410G>C (p.Glu470Asp) | |
12 | g.52447792C>T | CA480068864 | KRT6B | c.1410G>A (p.Glu470=) | gnomAD v4 |
12 | g.52447793T>A | CA384981770 | KRT6B | c.1409A>T (p.Glu470Val) | |
12 | g.52447793T>C | CA384981772 | KRT6B | c.1409A>G (p.Glu470Gly) | |
12 | g.52447793T>G | CA384981776 | KRT6B | c.1409A>C (p.Glu470Ala) | |
12 | g.52447794C>A | CA384981780 | KRT6B | c.1408G>T (p.Glu470Ter) | |
12 | g.52447794C>G | CA384981781 | KRT6B | c.1408G>C (p.Glu470Gln) | |
12 | g.52447794C>T | CA384981783 | KRT6B | c.1408G>A (p.Glu470Lys) | |
12 | g.52447795C>A | CA480068868 | KRT6B | c.1407G>T (p.Leu469=) | |
12 | g.52447795C>G | CA480068869 | KRT6B | c.1407G>C (p.Leu469=) | |
12 | g.52447795C>T | CA480068870 | KRT6B | c.1407G>A (p.Leu469=) | |
12 | g.52447796A= | CA2036494013 | KRT6B | c.1406T= (p.Leu469=) | |
12 | g.52447796A>C | CA384981786 | KRT6B | c.1406T>G (p.Leu469Arg) | ClinVar dbSNP |
12 | g.52447796A>G | CA384981787 | KRT6B | c.1406T>C (p.Leu469Pro) | |
12 | g.52447796A>T | CA384981788 | KRT6B | c.1406T>A (p.Leu469Gln) | |
12 | g.52447797G>A | CA480068872 | KRT6B | c.1405C>T (p.Leu469=) | gnomAD v4 |
12 | g.52447797G>C | CA384981789 | KRT6B | c.1405C>G (p.Leu469Val) | |
12 | g.52447797G>T | CA384981790 | KRT6B | c.1405C>A (p.Leu469Met) | |
12 | g.52447798C>A | CA480068873 | KRT6B | c.1404G>T (p.Leu468=) | |
12 | g.52447798C= | CA2036494021 | KRT6B | c.1404G= (p.Leu468=) | |
12 | g.52447798C>G | CA480068875 | KRT6B | c.1404G>C (p.Leu468=) | |
12 | g.52447798C>T | CA480068877 | KRT6B | c.1404G>A (p.Leu468=) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.52447799A>C | CA384981793 | KRT6B | c.1403T>G (p.Leu468Arg) | |
12 | g.52447799A>G | CA384981797 | KRT6B | c.1403T>C (p.Leu468Pro) | |
12 | g.52447799A>T | CA384981794 | KRT6B | c.1403T>A (p.Leu468Gln) | |
12 | g.52447800G>A | CA480068879 | KRT6B | c.1402C>T (p.Leu468=) | gnomAD v4 |
12 | g.52447800G>C | CA384981799 | KRT6B | c.1402C>G (p.Leu468Val) | |
12 | g.52447800G>T | CA384981800 | KRT6B | c.1402C>A (p.Leu468Met) | |
12 | g.52447801C>A | CA384981803 | KRT6B | c.1401G>T (p.Lys467Asn) | |
12 | g.52447801C>G | CA384981805 | KRT6B | c.1401G>C (p.Lys467Asn) | |
12 | g.52447801C>T | CA480068880 | KRT6B | c.1401G>A (p.Lys467=) | gnomAD v4 |
12 | g.52447802T>A | CA384981807 | KRT6B | c.1400A>T (p.Lys467Met) | |
12 | g.52447802T>C | CA384981809 | KRT6B | c.1400A>G (p.Lys467Arg) |