Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.46016279T>ACA409227500MMP9,SLC12A5-AS1c.2035T>A (p.Tyr679Asn)
n.669-1491A>T
20g.46016279T>CCA409227502MMP9,SLC12A5-AS1c.2035T>C (p.Tyr679His)
n.669-1491A>G
dbSNP gnomAD v3 gnomAD v4 COSMIC
20g.46016279T>GCA409227505MMP9,SLC12A5-AS1c.2035T>G (p.Tyr679Asp)
n.669-1491A>C
20g.46016279T=CA2366481064MMP9,SLC12A5-AS1c.2035T= (p.Tyr679=)
n.669-1491A=
20g.46016280A=CA2366481065MMP9,SLC12A5-AS1c.2036A= (p.Tyr679=)
n.669-1492T=
20g.46016280A>CCA409227508MMP9,SLC12A5-AS1c.2036A>C (p.Tyr679Ser)
n.669-1492T>G
20g.46016280A>GCA409227510MMP9,SLC12A5-AS1c.2036A>G (p.Tyr679Cys)
n.669-1492T>C
dbSNP gnomAD v4
20g.46016280A>TCA409227522MMP9,SLC12A5-AS1c.2036A>T (p.Tyr679Phe)
n.669-1492T>A
20g.46016281C>ACA409227527MMP9,SLC12A5-AS1c.2037C>A (p.Tyr679Ter)
n.669-1493G>T
20g.46016281C>GCA409227529MMP9,SLC12A5-AS1c.2037C>G (p.Tyr679Ter)
n.669-1493G>C
20g.46016281C>TCA510650587MMP9,SLC12A5-AS1c.2037C>T (p.Tyr679=)
n.669-1493G>A
20g.46016282T>ACA409227541MMP9,SLC12A5-AS1c.2038T>A (p.Trp680Arg)
n.669-1494A>T
20g.46016282T>CCA409227538MMP9,SLC12A5-AS1c.2038T>C (p.Trp680Arg)
n.669-1494A>G
gnomAD v4
20g.46016282T>GCA409227539MMP9,SLC12A5-AS1c.2038T>G (p.Trp680Gly)
n.669-1494A>C
20g.46016283G>ACA409227542MMP9,SLC12A5-AS1c.2039G>A (p.Trp680Ter)
n.669-1495C>T
20g.46016283G>CCA409227543MMP9,SLC12A5-AS1c.2039G>C (p.Trp680Ser)
n.669-1495C>G
20g.46016283G>TCA409227546MMP9,SLC12A5-AS1c.2039G>T (p.Trp680Leu)
n.669-1495C>A
20g.46016284G>ACA409227556MMP9,SLC12A5-AS1c.2040G>A (p.Trp680Ter)
n.669-1496C>T
COSMIC
20g.46016284G>CCA409227559MMP9,SLC12A5-AS1c.2040G>C (p.Trp680Cys)
n.669-1496C>G
20g.46016284G>TCA409227563MMP9,SLC12A5-AS1c.2040G>T (p.Trp680Cys)
n.669-1496C>A
20g.46016285C>ACA409227574MMP9,SLC12A5-AS1c.2041C>A (p.Arg681Ser)
n.669-1497G>T
gnomAD v4
20g.46016285C=CA2366481066MMP9,SLC12A5-AS1c.2041C= (p.Arg681=)
n.669-1497G=
20g.46016285C>GCA409227576MMP9,SLC12A5-AS1c.2041C>G (p.Arg681Gly)
n.669-1497G>C
dbSNP gnomAD v2 gnomAD v4
20g.46016285C>TCA9886881MMP9,SLC12A5-AS1c.2041C>T (p.Arg681Cys)
n.669-1497G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016286G>ACA9886882MMP9,SLC12A5-AS1c.2042G>A (p.Arg681His)
n.669-1498C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
20g.46016286G>CCA409227599MMP9,SLC12A5-AS1c.2042G>C (p.Arg681Pro)
n.669-1498C>G
20g.46016286G=CA2366481067MMP9,SLC12A5-AS1c.2042G= (p.Arg681=)
n.669-1498C=
20g.46016286G>TCA409227606MMP9,SLC12A5-AS1c.2042G>T (p.Arg681Leu)
n.669-1498C>A
20g.46016286dupCA2653117264MMP9,SLC12A5-AS1c.2042dup (p.Val682ArgfsTer6)
n.669-1498dup
gnomAD v4
20g.46016287C>ACA510650599MMP9,SLC12A5-AS1c.2043C>A (p.Arg681=)
n.669-1499G>T
20g.46016287C=CA2366481068MMP9,SLC12A5-AS1c.2043C= (p.Arg681=)
n.669-1499G=
20g.46016287C>GCA510650597MMP9,SLC12A5-AS1c.2043C>G (p.Arg681=)
n.669-1499G>C
20g.46016287C>TCA9886883MMP9,SLC12A5-AS1c.2043C>T (p.Arg681=)
n.669-1499G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016287_46016289delinsCGTCA2366481069MMP9,SLC12A5-AS1c.2043_2045delinsCGT (p.Arg681=)
n.669-1501_669-1499delinsACG
20g.46016288G>ACA9886884MMP9,SLC12A5-AS1c.2044G>A (p.Val682Met)
n.669-1500C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
20g.46016288G>CCA409227614MMP9,SLC12A5-AS1c.2044G>C (p.Val682Leu)
n.669-1500C>G
gnomAD v4
20g.46016288G=CA2366481071MMP9,SLC12A5-AS1c.2044G= (p.Val682=)
n.669-1500C=
20g.46016288G>TCA9886885MMP9,SLC12A5-AS1c.2044G>T (p.Val682Leu)
n.669-1500C>A
dbSNP ExAC gnomAD v2 gnomAD v4
20g.46016289_46016290delCA2366481070MMP9,SLC12A5-AS1c.2045_2046del (p.Val682GlufsTer5)
n.669-1501_669-1500del
dbSNP
20g.46016289T>ACA409227619MMP9,SLC12A5-AS1c.2045T>A (p.Val682Glu)
n.669-1501A>T
20g.46016289T>CCA409227621MMP9,SLC12A5-AS1c.2045T>C (p.Val682Ala)
n.669-1501A>G
gnomAD v4
20g.46016289T>GCA409227622MMP9,SLC12A5-AS1c.2045T>G (p.Val682Gly)
n.669-1501A>C
gnomAD v4
20g.46016290G>ACA510650604MMP9,SLC12A5-AS1c.2046G>A (p.Val682=)
n.669-1502C>T
20g.46016290G>CCA510650606MMP9,SLC12A5-AS1c.2046G>C (p.Val682=)
n.669-1502C>G
20g.46016290G>TCA510650607MMP9,SLC12A5-AS1c.2046G>T (p.Val682=)
n.669-1502C>A
20g.46016291A>CCA409227625MMP9,SLC12A5-AS1c.2047A>C (p.Ser683Arg)
n.669-1503T>G
20g.46016291A>GCA409227627MMP9,SLC12A5-AS1c.2047A>G (p.Ser683Gly)
n.669-1503T>C
20g.46016291A>TCA409227630MMP9,SLC12A5-AS1c.2047A>T (p.Ser683Cys)
n.669-1503T>A
20g.46016292G>ACA409227635MMP9,SLC12A5-AS1c.2048G>A (p.Ser683Asn)
n.669-1504C>T
gnomAD v4
20g.46016292G>CCA409227636MMP9,SLC12A5-AS1c.2048G>C (p.Ser683Thr)
n.669-1504C>G
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched