Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
20 | g.46016321C= | CA2366481084 | MMP9,SLC12A5-AS1 | c.2077C= (p.Gln693=) n.669-1533G= | |
20 | g.46016321C>G | CA409227981 | MMP9,SLC12A5-AS1 | c.2077C>G (p.Gln693Glu) n.669-1533G>C | |
20 | g.46016321C>T | CA409227985 | MMP9,SLC12A5-AS1 | c.2077C>T (p.Gln693Ter) n.669-1533G>A | dbSNP gnomAD v4 |
20 | g.46016321_46016324del | CA2741670583 | MMP9,SLC12A5-AS1 | c.2077_2080del (p.Gln693TrpfsTer4) n.669-1536_669-1533del | |
20 | g.46016322A= | CA2366481085 | MMP9,SLC12A5-AS1 | c.2078A= (p.Gln693=) n.669-1534T= | |
20 | g.46016322A>C | CA409227992 | MMP9,SLC12A5-AS1 | c.2078A>C (p.Gln693Pro) n.669-1534T>G | |
20 | g.46016322A>G | CA9886896 | MMP9,SLC12A5-AS1 | c.2078A>G (p.Gln693Arg) n.669-1534T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016322A>T | CA409227998 | MMP9,SLC12A5-AS1 | c.2078A>T (p.Gln693Leu) n.669-1534T>A | gnomAD v4 |
20 | g.46016323A>C | CA409228001 | MMP9,SLC12A5-AS1 | c.2079A>C (p.Gln693His) n.669-1535T>G | |
20 | g.46016323A>G | CA510650704 | MMP9,SLC12A5-AS1 | c.2079A>G (p.Gln693=) n.669-1535T>C | |
20 | g.46016323A>T | CA409228003 | MMP9,SLC12A5-AS1 | c.2079A>T (p.Gln693His) n.669-1535T>A | |
20 | g.46016324G>A | CA409228013 | MMP9,SLC12A5-AS1 | c.2080G>A (p.Val694Met) n.669-1536C>T | |
20 | g.46016324G>C | CA409228015 | MMP9,SLC12A5-AS1 | c.2080G>C (p.Val694Leu) n.669-1536C>G | |
20 | g.46016324G>T | CA409228018 | MMP9,SLC12A5-AS1 | c.2080G>T (p.Val694Leu) n.669-1536C>A | |
20 | g.46016325T>A | CA409228023 | MMP9,SLC12A5-AS1 | c.2081T>A (p.Val694Glu) n.669-1537A>T | |
20 | g.46016325T>C | CA409228024 | MMP9,SLC12A5-AS1 | c.2081T>C (p.Val694Ala) n.669-1537A>G | dbSNP |
20 | g.46016325T>G | CA409228026 | MMP9,SLC12A5-AS1 | c.2081T>G (p.Val694Gly) n.669-1537A>C | gnomAD v4 |
20 | g.46016325T= | CA2366481086 | MMP9,SLC12A5-AS1 | c.2081T= (p.Val694=) n.669-1537A= | |
20 | g.46016326G>A | CA9886897 | MMP9,SLC12A5-AS1 | c.2082G>A (p.Val694=) n.669-1538C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016326G>C | CA510650710 | MMP9,SLC12A5-AS1 | c.2082G>C (p.Val694=) n.669-1538C>G | |
20 | g.46016326G= | CA2366481087 | MMP9,SLC12A5-AS1 | c.2082G= (p.Val694=) n.669-1538C= | |
20 | g.46016326G>T | CA510650711 | MMP9,SLC12A5-AS1 | c.2082G>T (p.Val694=) n.669-1538C>A | |
20 | g.46016327G>A | CA409228050 | MMP9,SLC12A5-AS1 | c.2083G>A (p.Gly695Ser) n.669-1539C>T | |
20 | g.46016327G>C | CA409228051 | MMP9,SLC12A5-AS1 | c.2083G>C (p.Gly695Arg) n.669-1539C>G | |
20 | g.46016327G>T | CA409228049 | MMP9,SLC12A5-AS1 | c.2083G>T (p.Gly695Cys) n.669-1539C>A | |
20 | g.46016328G>A | CA409228052 | MMP9,SLC12A5-AS1 | c.2084G>A (p.Gly695Asp) n.669-1540C>T | |
20 | g.46016328G>C | CA409228053 | MMP9,SLC12A5-AS1 | c.2084G>C (p.Gly695Ala) n.669-1540C>G | |
20 | g.46016328G>T | CA409228057 | MMP9,SLC12A5-AS1 | c.2084G>T (p.Gly695Val) n.669-1540C>A | |
20 | g.46016329C>A | CA510650719 | MMP9,SLC12A5-AS1 | c.2085C>A (p.Gly695=) n.669-1541G>T | |
20 | g.46016329C= | CA2366481088 | MMP9,SLC12A5-AS1 | c.2085C= (p.Gly695=) n.669-1541G= | |
20 | g.46016329C>G | CA9886898 | MMP9,SLC12A5-AS1 | c.2085C>G (p.Gly695=) n.669-1541G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
20 | g.46016329C>T | CA510650722 | MMP9,SLC12A5-AS1 | c.2085C>T (p.Gly695=) n.669-1541G>A | |
20 | g.46016330T>A | CA409228086 | MMP9,SLC12A5-AS1 | c.2086T>A (p.Tyr696Asn) n.669-1542A>T | |
20 | g.46016330T>C | CA409228082 | MMP9,SLC12A5-AS1 | c.2086T>C (p.Tyr696His) n.669-1542A>G | |
20 | g.46016330T>G | CA409228079 | MMP9,SLC12A5-AS1 | c.2086T>G (p.Tyr696Asp) n.669-1542A>C | gnomAD v4 |
20 | g.46016331A>C | CA409228089 | MMP9,SLC12A5-AS1 | c.2087A>C (p.Tyr696Ser) n.669-1543T>G | |
20 | g.46016331A>G | CA409228091 | MMP9,SLC12A5-AS1 | c.2087A>G (p.Tyr696Cys) n.669-1543T>C | |
20 | g.46016331A>T | CA409228098 | MMP9,SLC12A5-AS1 | c.2087A>T (p.Tyr696Phe) n.669-1543T>A | |
20 | g.46016332C>A | CA409228101 | MMP9,SLC12A5-AS1 | c.2088C>A (p.Tyr696Ter) n.669-1544G>T | |
20 | g.46016332C= | CA2366481089 | MMP9,SLC12A5-AS1 | c.2088C= (p.Tyr696=) n.669-1544G= | |
20 | g.46016332C>G | CA409228105 | MMP9,SLC12A5-AS1 | c.2088C>G (p.Tyr696Ter) n.669-1544G>C | |
20 | g.46016332C>T | CA9886899 | MMP9,SLC12A5-AS1 | c.2088C>T (p.Tyr696=) n.669-1544G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
20 | g.46016333G>A | CA9886900 | MMP9,SLC12A5-AS1 | c.2089G>A (p.Val697Met) n.669-1545C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
20 | g.46016333G>C | CA409228113 | MMP9,SLC12A5-AS1 | c.2089G>C (p.Val697Leu) n.669-1545C>G | |
20 | g.46016333G= | CA2366481090 | MMP9,SLC12A5-AS1 | c.2089G= (p.Val697=) n.669-1545C= | |
20 | g.46016333G>T | CA409228111 | MMP9,SLC12A5-AS1 | c.2089G>T (p.Val697Leu) n.669-1545C>A |