Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46016307T>ACA409227830MMP9,SLC12A5-AS1c.2063T>A (p.Leu688Ter)
n.669-1519A>T
20g.46016307T>CCA9886891MMP9,SLC12A5-AS1c.2063T>C (p.Leu688Ser)
n.669-1519A>G
dbSNP ExAC gnomAD v2
20g.46016307T>GCA409227828MMP9,SLC12A5-AS1c.2063T>G (p.Leu688Trp)
n.669-1519A>C
20g.46016307T=CA2366481078MMP9,SLC12A5-AS1c.2063T= (p.Leu688=)
n.669-1519A=
20g.46016308G>ACA510650658MMP9,SLC12A5-AS1c.2064G>A (p.Leu688=)
n.669-1520C>T
20g.46016308G>CCA409227841MMP9,SLC12A5-AS1c.2064G>C (p.Leu688Phe)
n.669-1520C>G
20g.46016308G>TCA409227845MMP9,SLC12A5-AS1c.2064G>T (p.Leu688Phe)
n.669-1520C>A
20g.46016309A>CCA409227857MMP9,SLC12A5-AS1c.2065A>C (p.Asn689His)
n.669-1521T>G
20g.46016309A>GCA409227862MMP9,SLC12A5-AS1c.2065A>G (p.Asn689Asp)
n.669-1521T>C
20g.46016309A>TCA409227866MMP9,SLC12A5-AS1c.2065A>T (p.Asn689Tyr)
n.669-1521T>A
20g.46016310A=CA2366481079MMP9,SLC12A5-AS1c.2066A= (p.Asn689=)
n.669-1522T=
20g.46016310A>CCA409227875MMP9,SLC12A5-AS1c.2066A>C (p.Asn689Thr)
n.669-1522T>G
20g.46016310A>GCA409227870MMP9,SLC12A5-AS1c.2066A>G (p.Asn689Ser)
n.669-1522T>C
20g.46016310A>TCA9886892MMP9,SLC12A5-AS1c.2066A>T (p.Asn689Ile)
n.669-1522T>A
dbSNP ExAC gnomAD v2 gnomAD v4
20g.46016311C>ACA409227881MMP9,SLC12A5-AS1c.2067C>A (p.Asn689Lys)
n.669-1523G>T
gnomAD v4
20g.46016311C>GCA409227889MMP9,SLC12A5-AS1c.2067C>G (p.Asn689Lys)
n.669-1523G>C
20g.46016311C>TCA510650666MMP9,SLC12A5-AS1c.2067C>T (p.Asn689=)
n.669-1523G>A
20g.46016312C>ACA409227895MMP9,SLC12A5-AS1c.2068C>A (p.Gln690Lys)
n.669-1524G>T
gnomAD v4
20g.46016312C>GCA409227896MMP9,SLC12A5-AS1c.2068C>G (p.Gln690Glu)
n.669-1524G>C
gnomAD v4
20g.46016312C>TCA409227899MMP9,SLC12A5-AS1c.2068C>T (p.Gln690Ter)
n.669-1524G>A
20g.46016312_46016314delCA2741670582MMP9,SLC12A5-AS1c.2068_2070del (p.Gln690del)
n.669-1526_669-1524del
20g.46016313A>CCA409227905MMP9,SLC12A5-AS1c.2069A>C (p.Gln690Pro)
n.669-1525T>G
20g.46016313A>GCA409227903MMP9,SLC12A5-AS1c.2069A>G (p.Gln690Arg)
n.669-1525T>C
20g.46016313A>TCA409227901MMP9,SLC12A5-AS1c.2069A>T (p.Gln690Leu)
n.669-1525T>A
20g.46016314G>ACA510650673MMP9,SLC12A5-AS1c.2070G>A (p.Gln690=)
n.669-1526C>T
20g.46016314G>CCA409227907MMP9,SLC12A5-AS1c.2070G>C (p.Gln690His)
n.669-1526C>G
20g.46016314G>TCA409227910MMP9,SLC12A5-AS1c.2070G>T (p.Gln690His)
n.669-1526C>A
20g.46016315G>ACA409227918MMP9,SLC12A5-AS1c.2071G>A (p.Val691Met)
n.669-1527C>T
ClinVar dbSNP gnomAD v3 gnomAD v4
20g.46016315G>CCA9886893MMP9,SLC12A5-AS1c.2071G>C (p.Val691Leu)
n.669-1527C>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016315G=CA2366481080MMP9,SLC12A5-AS1c.2071G= (p.Val691=)
n.669-1527C=
20g.46016315G>TCA409227922MMP9,SLC12A5-AS1c.2071G>T (p.Val691Leu)
n.669-1527C>A
20g.46016316T>ACA409227938MMP9,SLC12A5-AS1c.2072T>A (p.Val691Glu)
n.669-1528A>T
20g.46016316T>CCA9886894MMP9,SLC12A5-AS1c.2072T>C (p.Val691Ala)
n.669-1528A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016316T>GCA409227949MMP9,SLC12A5-AS1c.2072T>G (p.Val691Gly)
n.669-1528A>C
gnomAD v4
20g.46016316T=CA2366481081MMP9,SLC12A5-AS1c.2072T= (p.Val691=)
n.669-1528A=
20g.46016317G>ACA510650682MMP9,SLC12A5-AS1c.2073G>A (p.Val691=)
n.669-1529C>T
20g.46016317G>CCA510650684MMP9,SLC12A5-AS1c.2073G>C (p.Val691=)
n.669-1529C>G
20g.46016317G>TCA510650685MMP9,SLC12A5-AS1c.2073G>T (p.Val691=)
n.669-1529C>A
20g.46016318G>ACA409227953MMP9,SLC12A5-AS1c.2074G>A (p.Asp692Asn)
n.669-1530C>T
ClinVar dbSNP
20g.46016318G>CCA9886895MMP9,SLC12A5-AS1c.2074G>C (p.Asp692His)
n.669-1530C>G
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
20g.46016318G=CA2366481082MMP9,SLC12A5-AS1c.2074G= (p.Asp692=)
n.669-1530C=
20g.46016318G>TCA409227954MMP9,SLC12A5-AS1c.2074G>T (p.Asp692Tyr)
n.669-1530C>A
20g.46016319A=CA2366481083MMP9,SLC12A5-AS1c.2075A= (p.Asp692=)
n.669-1531T=
20g.46016319A>CCA409227956MMP9,SLC12A5-AS1c.2075A>C (p.Asp692Ala)
n.669-1531T>G
20g.46016319A>GCA409227959MMP9,SLC12A5-AS1c.2075A>G (p.Asp692Gly)
n.669-1531T>C
20g.46016319A>TCA315639666MMP9,SLC12A5-AS1c.2075A>T (p.Asp692Val)
n.669-1531T>A
dbSNP gnomAD v4
20g.46016320C>ACA409227964MMP9,SLC12A5-AS1c.2076C>A (p.Asp692Glu)
n.669-1532G>T
20g.46016320C>GCA409227975MMP9,SLC12A5-AS1c.2076C>G (p.Asp692Glu)
n.669-1532G>C
20g.46016320C>TCA510650694MMP9,SLC12A5-AS1c.2076C>T (p.Asp692=)
n.669-1532G>A
20g.46016321C>ACA409227979MMP9,SLC12A5-AS1c.2077C>A (p.Gln693Lys)
n.669-1533G>T

Number of alleles fetched