Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
20 | g.46016307T>A | CA409227830 | MMP9,SLC12A5-AS1 | c.2063T>A (p.Leu688Ter) n.669-1519A>T | |
20 | g.46016307T>C | CA9886891 | MMP9,SLC12A5-AS1 | c.2063T>C (p.Leu688Ser) n.669-1519A>G | dbSNP ExAC gnomAD v2 |
20 | g.46016307T>G | CA409227828 | MMP9,SLC12A5-AS1 | c.2063T>G (p.Leu688Trp) n.669-1519A>C | |
20 | g.46016307T= | CA2366481078 | MMP9,SLC12A5-AS1 | c.2063T= (p.Leu688=) n.669-1519A= | |
20 | g.46016308G>A | CA510650658 | MMP9,SLC12A5-AS1 | c.2064G>A (p.Leu688=) n.669-1520C>T | |
20 | g.46016308G>C | CA409227841 | MMP9,SLC12A5-AS1 | c.2064G>C (p.Leu688Phe) n.669-1520C>G | |
20 | g.46016308G>T | CA409227845 | MMP9,SLC12A5-AS1 | c.2064G>T (p.Leu688Phe) n.669-1520C>A | |
20 | g.46016309A>C | CA409227857 | MMP9,SLC12A5-AS1 | c.2065A>C (p.Asn689His) n.669-1521T>G | |
20 | g.46016309A>G | CA409227862 | MMP9,SLC12A5-AS1 | c.2065A>G (p.Asn689Asp) n.669-1521T>C | |
20 | g.46016309A>T | CA409227866 | MMP9,SLC12A5-AS1 | c.2065A>T (p.Asn689Tyr) n.669-1521T>A | |
20 | g.46016310A= | CA2366481079 | MMP9,SLC12A5-AS1 | c.2066A= (p.Asn689=) n.669-1522T= | |
20 | g.46016310A>C | CA409227875 | MMP9,SLC12A5-AS1 | c.2066A>C (p.Asn689Thr) n.669-1522T>G | |
20 | g.46016310A>G | CA409227870 | MMP9,SLC12A5-AS1 | c.2066A>G (p.Asn689Ser) n.669-1522T>C | |
20 | g.46016310A>T | CA9886892 | MMP9,SLC12A5-AS1 | c.2066A>T (p.Asn689Ile) n.669-1522T>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016311C>A | CA409227881 | MMP9,SLC12A5-AS1 | c.2067C>A (p.Asn689Lys) n.669-1523G>T | gnomAD v4 |
20 | g.46016311C>G | CA409227889 | MMP9,SLC12A5-AS1 | c.2067C>G (p.Asn689Lys) n.669-1523G>C | |
20 | g.46016311C>T | CA510650666 | MMP9,SLC12A5-AS1 | c.2067C>T (p.Asn689=) n.669-1523G>A | |
20 | g.46016312C>A | CA409227895 | MMP9,SLC12A5-AS1 | c.2068C>A (p.Gln690Lys) n.669-1524G>T | gnomAD v4 |
20 | g.46016312C>G | CA409227896 | MMP9,SLC12A5-AS1 | c.2068C>G (p.Gln690Glu) n.669-1524G>C | gnomAD v4 |
20 | g.46016312C>T | CA409227899 | MMP9,SLC12A5-AS1 | c.2068C>T (p.Gln690Ter) n.669-1524G>A | |
20 | g.46016312_46016314del | CA2741670582 | MMP9,SLC12A5-AS1 | c.2068_2070del (p.Gln690del) n.669-1526_669-1524del | |
20 | g.46016313A>C | CA409227905 | MMP9,SLC12A5-AS1 | c.2069A>C (p.Gln690Pro) n.669-1525T>G | |
20 | g.46016313A>G | CA409227903 | MMP9,SLC12A5-AS1 | c.2069A>G (p.Gln690Arg) n.669-1525T>C | |
20 | g.46016313A>T | CA409227901 | MMP9,SLC12A5-AS1 | c.2069A>T (p.Gln690Leu) n.669-1525T>A | |
20 | g.46016314G>A | CA510650673 | MMP9,SLC12A5-AS1 | c.2070G>A (p.Gln690=) n.669-1526C>T | |
20 | g.46016314G>C | CA409227907 | MMP9,SLC12A5-AS1 | c.2070G>C (p.Gln690His) n.669-1526C>G | |
20 | g.46016314G>T | CA409227910 | MMP9,SLC12A5-AS1 | c.2070G>T (p.Gln690His) n.669-1526C>A | |
20 | g.46016315G>A | CA409227918 | MMP9,SLC12A5-AS1 | c.2071G>A (p.Val691Met) n.669-1527C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
20 | g.46016315G>C | CA9886893 | MMP9,SLC12A5-AS1 | c.2071G>C (p.Val691Leu) n.669-1527C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016315G= | CA2366481080 | MMP9,SLC12A5-AS1 | c.2071G= (p.Val691=) n.669-1527C= | |
20 | g.46016315G>T | CA409227922 | MMP9,SLC12A5-AS1 | c.2071G>T (p.Val691Leu) n.669-1527C>A | |
20 | g.46016316T>A | CA409227938 | MMP9,SLC12A5-AS1 | c.2072T>A (p.Val691Glu) n.669-1528A>T | |
20 | g.46016316T>C | CA9886894 | MMP9,SLC12A5-AS1 | c.2072T>C (p.Val691Ala) n.669-1528A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016316T>G | CA409227949 | MMP9,SLC12A5-AS1 | c.2072T>G (p.Val691Gly) n.669-1528A>C | gnomAD v4 |
20 | g.46016316T= | CA2366481081 | MMP9,SLC12A5-AS1 | c.2072T= (p.Val691=) n.669-1528A= | |
20 | g.46016317G>A | CA510650682 | MMP9,SLC12A5-AS1 | c.2073G>A (p.Val691=) n.669-1529C>T | |
20 | g.46016317G>C | CA510650684 | MMP9,SLC12A5-AS1 | c.2073G>C (p.Val691=) n.669-1529C>G | |
20 | g.46016317G>T | CA510650685 | MMP9,SLC12A5-AS1 | c.2073G>T (p.Val691=) n.669-1529C>A | |
20 | g.46016318G>A | CA409227953 | MMP9,SLC12A5-AS1 | c.2074G>A (p.Asp692Asn) n.669-1530C>T | ClinVar dbSNP |
20 | g.46016318G>C | CA9886895 | MMP9,SLC12A5-AS1 | c.2074G>C (p.Asp692His) n.669-1530C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016318G= | CA2366481082 | MMP9,SLC12A5-AS1 | c.2074G= (p.Asp692=) n.669-1530C= | |
20 | g.46016318G>T | CA409227954 | MMP9,SLC12A5-AS1 | c.2074G>T (p.Asp692Tyr) n.669-1530C>A | |
20 | g.46016319A= | CA2366481083 | MMP9,SLC12A5-AS1 | c.2075A= (p.Asp692=) n.669-1531T= | |
20 | g.46016319A>C | CA409227956 | MMP9,SLC12A5-AS1 | c.2075A>C (p.Asp692Ala) n.669-1531T>G | |
20 | g.46016319A>G | CA409227959 | MMP9,SLC12A5-AS1 | c.2075A>G (p.Asp692Gly) n.669-1531T>C | |
20 | g.46016319A>T | CA315639666 | MMP9,SLC12A5-AS1 | c.2075A>T (p.Asp692Val) n.669-1531T>A | dbSNP gnomAD v4 |
20 | g.46016320C>A | CA409227964 | MMP9,SLC12A5-AS1 | c.2076C>A (p.Asp692Glu) n.669-1532G>T | |
20 | g.46016320C>G | CA409227975 | MMP9,SLC12A5-AS1 | c.2076C>G (p.Asp692Glu) n.669-1532G>C | |
20 | g.46016320C>T | CA510650694 | MMP9,SLC12A5-AS1 | c.2076C>T (p.Asp692=) n.669-1532G>A | |
20 | g.46016321C>A | CA409227979 | MMP9,SLC12A5-AS1 | c.2077C>A (p.Gln693Lys) n.669-1533G>T |