Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46016324G>ACA409228013MMP9,SLC12A5-AS1c.2080G>A (p.Val694Met)
n.669-1536C>T
20g.46016324G>CCA409228015MMP9,SLC12A5-AS1c.2080G>C (p.Val694Leu)
n.669-1536C>G
20g.46016324G>TCA409228018MMP9,SLC12A5-AS1c.2080G>T (p.Val694Leu)
n.669-1536C>A
20g.46016325T>ACA409228023MMP9,SLC12A5-AS1c.2081T>A (p.Val694Glu)
n.669-1537A>T
20g.46016325T>CCA409228024MMP9,SLC12A5-AS1c.2081T>C (p.Val694Ala)
n.669-1537A>G
dbSNP
20g.46016325T>GCA409228026MMP9,SLC12A5-AS1c.2081T>G (p.Val694Gly)
n.669-1537A>C
gnomAD v4
20g.46016325T=CA2366481086MMP9,SLC12A5-AS1c.2081T= (p.Val694=)
n.669-1537A=
20g.46016326G>ACA9886897MMP9,SLC12A5-AS1c.2082G>A (p.Val694=)
n.669-1538C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016326G>CCA510650710MMP9,SLC12A5-AS1c.2082G>C (p.Val694=)
n.669-1538C>G
20g.46016326G=CA2366481087MMP9,SLC12A5-AS1c.2082G= (p.Val694=)
n.669-1538C=
20g.46016326G>TCA510650711MMP9,SLC12A5-AS1c.2082G>T (p.Val694=)
n.669-1538C>A
20g.46016327G>ACA409228050MMP9,SLC12A5-AS1c.2083G>A (p.Gly695Ser)
n.669-1539C>T
20g.46016327G>CCA409228051MMP9,SLC12A5-AS1c.2083G>C (p.Gly695Arg)
n.669-1539C>G
20g.46016327G>TCA409228049MMP9,SLC12A5-AS1c.2083G>T (p.Gly695Cys)
n.669-1539C>A
20g.46016328G>ACA409228052MMP9,SLC12A5-AS1c.2084G>A (p.Gly695Asp)
n.669-1540C>T
20g.46016328G>CCA409228053MMP9,SLC12A5-AS1c.2084G>C (p.Gly695Ala)
n.669-1540C>G
20g.46016328G>TCA409228057MMP9,SLC12A5-AS1c.2084G>T (p.Gly695Val)
n.669-1540C>A
20g.46016329C>ACA510650719MMP9,SLC12A5-AS1c.2085C>A (p.Gly695=)
n.669-1541G>T
20g.46016329C=CA2366481088MMP9,SLC12A5-AS1c.2085C= (p.Gly695=)
n.669-1541G=
20g.46016329C>GCA9886898MMP9,SLC12A5-AS1c.2085C>G (p.Gly695=)
n.669-1541G>C
dbSNP ExAC gnomAD v2 gnomAD v4
20g.46016329C>TCA510650722MMP9,SLC12A5-AS1c.2085C>T (p.Gly695=)
n.669-1541G>A
20g.46016330T>ACA409228086MMP9,SLC12A5-AS1c.2086T>A (p.Tyr696Asn)
n.669-1542A>T
20g.46016330T>CCA409228082MMP9,SLC12A5-AS1c.2086T>C (p.Tyr696His)
n.669-1542A>G
20g.46016330T>GCA409228079MMP9,SLC12A5-AS1c.2086T>G (p.Tyr696Asp)
n.669-1542A>C
gnomAD v4
20g.46016331A>CCA409228089MMP9,SLC12A5-AS1c.2087A>C (p.Tyr696Ser)
n.669-1543T>G
20g.46016331A>GCA409228091MMP9,SLC12A5-AS1c.2087A>G (p.Tyr696Cys)
n.669-1543T>C
20g.46016331A>TCA409228098MMP9,SLC12A5-AS1c.2087A>T (p.Tyr696Phe)
n.669-1543T>A
20g.46016332C>ACA409228101MMP9,SLC12A5-AS1c.2088C>A (p.Tyr696Ter)
n.669-1544G>T
20g.46016332C=CA2366481089MMP9,SLC12A5-AS1c.2088C= (p.Tyr696=)
n.669-1544G=
20g.46016332C>GCA409228105MMP9,SLC12A5-AS1c.2088C>G (p.Tyr696Ter)
n.669-1544G>C
20g.46016332C>TCA9886899MMP9,SLC12A5-AS1c.2088C>T (p.Tyr696=)
n.669-1544G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016333G>ACA9886900MMP9,SLC12A5-AS1c.2089G>A (p.Val697Met)
n.669-1545C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.46016333G>CCA409228113MMP9,SLC12A5-AS1c.2089G>C (p.Val697Leu)
n.669-1545C>G
20g.46016333G=CA2366481090MMP9,SLC12A5-AS1c.2089G= (p.Val697=)
n.669-1545C=
20g.46016333G>TCA409228111MMP9,SLC12A5-AS1c.2089G>T (p.Val697Leu)
n.669-1545C>A
20g.46016334T>ACA409228117MMP9,SLC12A5-AS1c.2090T>A (p.Val697Glu)
n.669-1546A>T
20g.46016334T>CCA409228119MMP9,SLC12A5-AS1c.2090T>C (p.Val697Ala)
n.669-1546A>G
20g.46016334T>GCA409228122MMP9,SLC12A5-AS1c.2090T>G (p.Val697Gly)
n.669-1546A>C
20g.46016335G>ACA510650738MMP9,SLC12A5-AS1c.2091G>A (p.Val697=)
n.669-1547C>T
20g.46016335G>CCA510650741MMP9,SLC12A5-AS1c.2091G>C (p.Val697=)
n.669-1547C>G
gnomAD v4
20g.46016335G>TCA510650743MMP9,SLC12A5-AS1c.2091G>T (p.Val697=)
n.669-1547C>A
20g.46016336A>CCA409228127MMP9,SLC12A5-AS1c.2092A>C (p.Thr698Pro)
n.669-1548T>G
20g.46016336A>GCA409228130MMP9,SLC12A5-AS1c.2092A>G (p.Thr698Ala)
n.669-1548T>C
20g.46016336A>TCA409228131MMP9,SLC12A5-AS1c.2092A>T (p.Thr698Ser)
n.669-1548T>A
20g.46016337C>ACA409228132MMP9,SLC12A5-AS1c.2093C>A (p.Thr698Asn)
n.669-1549G>T
20g.46016337C>GCA409228133MMP9,SLC12A5-AS1c.2093C>G (p.Thr698Ser)
n.669-1549G>C
20g.46016337C>TCA409228135MMP9,SLC12A5-AS1c.2093C>T (p.Thr698Ile)
n.669-1549G>A
gnomAD v4
20g.46016338C>ACA510650748MMP9,SLC12A5-AS1c.2094C>A (p.Thr698=)
n.669-1550G>T
20g.46016338C>GCA510650749MMP9,SLC12A5-AS1c.2094C>G (p.Thr698=)
n.669-1550G>C
20g.46016338C>TCA510650750MMP9,SLC12A5-AS1c.2094C>T (p.Thr698=)
n.669-1550G>A

Number of alleles fetched