Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
12 | g.5045728G>A | CA6399896 | KCNA5 | c.1581G>A (p.Thr527=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.5045728G>C | CA478096178 | KCNA5 | c.1581G>C (p.Thr527=) | |
12 | g.5045728G= | CA2013431361 | KCNA5 | c.1581G= (p.Thr527=) | |
12 | g.5045728G>T | CA478096176 | KCNA5 | c.1581G>T (p.Thr527=) | COSMIC |
12 | g.5045729G>A | CA383466794 | KCNA5 | c.1582G>A (p.Asp528Asn) | COSMIC |
12 | g.5045729G>C | CA383466795 | KCNA5 | c.1582G>C (p.Asp528His) | |
12 | g.5045729G>T | CA383466796 | KCNA5 | c.1582G>T (p.Asp528Tyr) | |
12 | g.5045730A>C | CA383466797 | KCNA5 | c.1583A>C (p.Asp528Ala) | |
12 | g.5045730A>G | CA383466798 | KCNA5 | c.1583A>G (p.Asp528Gly) | |
12 | g.5045730A>T | CA383466799 | KCNA5 | c.1583A>T (p.Asp528Val) | |
12 | g.5045731T>A | CA383466801 | KCNA5 | c.1584T>A (p.Asp528Glu) | |
12 | g.5045731T>C | CA478096183 | KCNA5 | c.1584T>C (p.Asp528=) | |
12 | g.5045731T>G | CA383466800 | KCNA5 | c.1584T>G (p.Asp528Glu) | |
12 | g.5045732C>A | CA383466802 | KCNA5 | c.1585C>A (p.His529Asn) | gnomAD v4 |
12 | g.5045732C>G | CA383466804 | KCNA5 | c.1585C>G (p.His529Asp) | |
12 | g.5045732C>T | CA383466803 | KCNA5 | c.1585C>T (p.His529Tyr) | |
12 | g.5045733A= | CA2013431362 | KCNA5 | c.1586A= (p.His529=) | |
12 | g.5045733A>C | CA383466805 | KCNA5 | c.1586A>C (p.His529Pro) | dbSNP gnomAD v4 |
12 | g.5045733A>G | CA383466806 | KCNA5 | c.1586A>G (p.His529Arg) | |
12 | g.5045733A>T | CA383466807 | KCNA5 | c.1586A>T (p.His529Leu) | |
12 | g.5045734C>A | CA383466808 | KCNA5 | c.1587C>A (p.His529Gln) | COSMIC |
12 | g.5045734C= | CA2013431363 | KCNA5 | c.1587C= (p.His529=) | |
12 | g.5045734C>G | CA383466809 | KCNA5 | c.1587C>G (p.His529Gln) | gnomAD v4 |
12 | g.5045734C>T | CA6399897 | KCNA5 | c.1587C>T (p.His529=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
12 | g.5045735G>A | CA231869110 | KCNA5 | c.1588G>A (p.Glu530Lys) | ClinVar dbSNP gnomAD v4 |
12 | g.5045735G>C | CA231869109 | KCNA5 | c.1588G>C (p.Glu530Gln) | dbSNP gnomAD v3 gnomAD v4 |
12 | g.5045735G= | CA2013431364 | KCNA5 | c.1588G= (p.Glu530=) | |
12 | g.5045735G>T | CA383466810 | KCNA5 | c.1588G>T (p.Glu530Ter) | ClinVar dbSNP |
12 | g.5045736A>C | CA383466811 | KCNA5 | c.1589A>C (p.Glu530Ala) | |
12 | g.5045736A>G | CA383466812 | KCNA5 | c.1589A>G (p.Glu530Gly) | |
12 | g.5045736A>T | CA383466813 | KCNA5 | c.1589A>T (p.Glu530Val) | |
12 | g.5045737G>A | CA478096192 | KCNA5 | c.1590G>A (p.Glu530=) | dbSNP gnomAD v4 |
12 | g.5045737G>C | CA383466814 | KCNA5 | c.1590G>C (p.Glu530Asp) | |
12 | g.5045737G= | CA2013431365 | KCNA5 | c.1590G= (p.Glu530=) | |
12 | g.5045737G>T | CA383466815 | KCNA5 | c.1590G>T (p.Glu530Asp) | |
12 | g.5045738G>A | CA383466816 | KCNA5 | c.1591G>A (p.Glu531Lys) | |
12 | g.5045738G>C | CA383466818 | KCNA5 | c.1591G>C (p.Glu531Gln) | gnomAD v4 |
12 | g.5045738G>T | CA383466817 | KCNA5 | c.1591G>T (p.Glu531Ter) | |
12 | g.5045739A>C | CA383466819 | KCNA5 | c.1592A>C (p.Glu531Ala) | |
12 | g.5045739A>G | CA383466820 | KCNA5 | c.1592A>G (p.Glu531Gly) | gnomAD v4 |
12 | g.5045739A>T | CA383466821 | KCNA5 | c.1592A>T (p.Glu531Val) | |
12 | g.5045740G>A | CA478096197 | KCNA5 | c.1593G>A (p.Glu531=) | |
12 | g.5045740G>C | CA383466822 | KCNA5 | c.1593G>C (p.Glu531Asp) | |
12 | g.5045740G>T | CA383466823 | KCNA5 | c.1593G>T (p.Glu531Asp) | |
12 | g.5045741C>A | CA383466824 | KCNA5 | c.1594C>A (p.Pro532Thr) | |
12 | g.5045741C>G | CA383466825 | KCNA5 | c.1594C>G (p.Pro532Ala) | |
12 | g.5045741C>T | CA383466826 | KCNA5 | c.1594C>T (p.Pro532Ser) | |
12 | g.5045742C>A | CA383466827 | KCNA5 | c.1595C>A (p.Pro532Gln) | |
12 | g.5045742C= | CA2013431366 | KCNA5 | c.1595C= (p.Pro532=) | |
12 | g.5045742C>G | CA383466828 | KCNA5 | c.1595C>G (p.Pro532Arg) |