Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.72007583_72007607dup | CA2609581014 | CHST3 | c.552_576dup (p.Lys193GlyfsTer?) | gnomAD v4 |
10 | g.72007594_72007596del | CA2722101866 | CHST3 | c.563_565del (p.Tyr188_Arg189delinsCys) | dbSNP |
10 | g.72007595C>A | CA377144742 | CHST3 | c.564C>A (p.Tyr188Ter) | |
10 | g.72007595C= | CA1918975935 | CHST3 | c.564C= (p.Tyr188=) | |
10 | g.72007595C>G | CA377144743 | CHST3 | c.564C>G (p.Tyr188Ter) | |
10 | g.72007595C>T | CA470284055 | CHST3 | c.564C>T (p.Tyr188=) | dbSNP |
10 | g.72007596C>A | CA377144745 | CHST3 | c.565C>A (p.Arg189Ser) | gnomAD v4 |
10 | g.72007596C>G | CA377144748 | CHST3 | c.565C>G (p.Arg189Gly) | |
10 | g.72007596C>T | CA377144749 | CHST3 | c.565C>T (p.Arg189Cys) | gnomAD v4 |
10 | g.72007597G>A | CA377144755 | CHST3 | c.566G>A (p.Arg189His) | dbSNP gnomAD v4 COSMIC |
10 | g.72007597G>C | CA377144758 | CHST3 | c.566G>C (p.Arg189Pro) | gnomAD v4 |
10 | g.72007597G= | CA1918975938 | CHST3 | c.566G= (p.Arg189=) | |
10 | g.72007597G>T | CA377144760 | CHST3 | c.566G>T (p.Arg189Leu) | dbSNP gnomAD v4 |
10 | g.72007598C>A | CA470284061 | CHST3 | c.567C>A (p.Arg189=) | |
10 | g.72007598C>G | CA470284062 | CHST3 | c.567C>G (p.Arg189=) | |
10 | g.72007598C>T | CA470284064 | CHST3 | c.567C>T (p.Arg189=) | gnomAD v4 COSMIC |
10 | g.72007600_72007602dup | CA2574581748 | CHST3 | c.569_571dup (p.Asp190_Val191insAsp) | |
10 | g.72007599G>A | CA377144775 | CHST3 | c.568G>A (p.Asp190Asn) | dbSNP gnomAD v4 |
10 | g.72007599G>C | CA377144771 | CHST3 | c.568G>C (p.Asp190His) | |
10 | g.72007599G= | CA1918975943 | CHST3 | c.568G= (p.Asp190=) | |
10 | g.72007599G>T | CA377144767 | CHST3 | c.568G>T (p.Asp190Tyr) | |
10 | g.72007600A>C | CA377144781 | CHST3 | c.569A>C (p.Asp190Ala) | |
10 | g.72007600A>G | CA377144789 | CHST3 | c.569A>G (p.Asp190Gly) | |
10 | g.72007600A>T | CA377144799 | CHST3 | c.569A>T (p.Asp190Val) | |
10 | g.72007601C>A | CA5548129 | CHST3 | c.570C>A (p.Asp190Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.72007601C= | CA1918975949 | CHST3 | c.570C= (p.Asp190=) | |
10 | g.72007601C>G | CA377144808 | CHST3 | c.570C>G (p.Asp190Glu) | dbSNP gnomAD v4 |
10 | g.72007601C>T | CA5548128 | CHST3 | c.570C>T (p.Asp190=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
10 | g.72007602G>A | CA377144827 | CHST3 | c.571G>A (p.Val191Met) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
10 | g.72007602G>C | CA377144823 | CHST3 | c.571G>C (p.Val191Leu) | |
10 | g.72007602G= | CA1918975952 | CHST3 | c.571G= (p.Val191=) | |
10 | g.72007602G>T | CA5548130 | CHST3 | c.571G>T (p.Val191Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
10 | g.72007603T>A | CA377144829 | CHST3 | c.572T>A (p.Val191Glu) | |
10 | g.72007603T>C | CA377144830 | CHST3 | c.572T>C (p.Val191Ala) | |
10 | g.72007603T>G | CA377144833 | CHST3 | c.572T>G (p.Val191Gly) | |
10 | g.72007604G>A | CA470284083 | CHST3 | c.573G>A (p.Val191=) | gnomAD v4 |
10 | g.72007604G>C | CA470284084 | CHST3 | c.573G>C (p.Val191=) | |
10 | g.72007604G>T | CA470284085 | CHST3 | c.573G>T (p.Val191=) | gnomAD v4 |
10 | g.72007605C>A | CA377144838 | CHST3 | c.574C>A (p.Leu192Ile) | |
10 | g.72007605C= | CA1918975956 | CHST3 | c.574C= (p.Leu192=) | |
10 | g.72007605C>G | CA377144839 | CHST3 | c.574C>G (p.Leu192Val) | dbSNP gnomAD v4 |
10 | g.72007605C>T | CA377144842 | CHST3 | c.574C>T (p.Leu192Phe) | dbSNP gnomAD v2 gnomAD v4 |
10 | g.72007606T>A | CA377144847 | CHST3 | c.575T>A (p.Leu192His) | |
10 | g.72007606T>C | CA377144857 | CHST3 | c.575T>C (p.Leu192Pro) | dbSNP |
10 | g.72007606T>G | CA377144850 | CHST3 | c.575T>G (p.Leu192Arg) | |
10 | g.72007606T= | CA1918975960 | CHST3 | c.575T= (p.Leu192=) | |
10 | g.72007607C>A | CA470284087 | CHST3 | c.576C>A (p.Leu192=) | gnomAD v4 |
10 | g.72007607C>G | CA470284089 | CHST3 | c.576C>G (p.Leu192=) | |
10 | g.72007607C>T | CA470284088 | CHST3 | c.576C>T (p.Leu192=) | gnomAD v4 |
10 | g.72007608A= | CA1918975965 | CHST3 | c.577A= (p.Lys193=) |