Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.46016333_46016336delCA2741670584MMP9,SLC12A5-AS1c.2089_2092del (p.Val697ProfsTer?)
n.669-1548_669-1545del
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
20g.46016339T>ACA409228139MMP9,SLC12A5-AS1c.2095T>A (p.Tyr699Asn)
n.669-1551A>T
20g.46016339T>CCA409228142MMP9,SLC12A5-AS1c.2095T>C (p.Tyr699His)
n.669-1551A>G
gnomAD v4
20g.46016339T>GCA409228145MMP9,SLC12A5-AS1c.2095T>G (p.Tyr699Asp)
n.669-1551A>C
20g.46016339_46016342delCA2741670585MMP9,SLC12A5-AS1c.2095_2098del (p.Tyr699ThrfsTer?)
n.669-1554_669-1551del
20g.46016340A>CCA409228154MMP9,SLC12A5-AS1c.2096A>C (p.Tyr699Ser)
n.669-1552T>G
20g.46016340A>GCA409228158MMP9,SLC12A5-AS1c.2096A>G (p.Tyr699Cys)
n.669-1552T>C
dbSNP gnomAD v3
20g.46016340A>TCA409228151MMP9,SLC12A5-AS1c.2096A>T (p.Tyr699Phe)
n.669-1552T>A
20g.46016341T>ACA409228161MMP9,SLC12A5-AS1c.2097T>A (p.Tyr699Ter)
n.669-1553A>T
20g.46016341T>CCA510650759MMP9,SLC12A5-AS1c.2097T>C (p.Tyr699=)
n.669-1553A>G
20g.46016341T>GCA409228164MMP9,SLC12A5-AS1c.2097T>G (p.Tyr699Ter)
n.669-1553A>C
20g.46016342G>ACA409228168MMP9,SLC12A5-AS1c.2098G>A (p.Asp700Asn)
n.669-1554C>T
20g.46016342G>CCA409228171MMP9,SLC12A5-AS1c.2098G>C (p.Asp700His)
n.669-1554C>G
20g.46016342G>TCA409228179MMP9,SLC12A5-AS1c.2098G>T (p.Asp700Tyr)
n.669-1554C>A
20g.46016343A>CCA409228182MMP9,SLC12A5-AS1c.2099A>C (p.Asp700Ala)
n.669-1555T>G
20g.46016343A>GCA409228193MMP9,SLC12A5-AS1c.2099A>G (p.Asp700Gly)
n.669-1555T>C
20g.46016343A>TCA409228198MMP9,SLC12A5-AS1c.2099A>T (p.Asp700Val)
n.669-1555T>A
20g.46016344C>ACA409228201MMP9,SLC12A5-AS1c.2100C>A (p.Asp700Glu)
n.669-1556G>T
20g.46016344C>GCA409228202MMP9,SLC12A5-AS1c.2100C>G (p.Asp700Glu)
n.669-1556G>C
20g.46016344C>TCA510650767MMP9,SLC12A5-AS1c.2100C>T (p.Asp700=)
n.669-1556G>A
gnomAD v4
20g.46016345A>CCA409228203MMP9,SLC12A5-AS1c.2101A>C (p.Ile701Leu)
n.669-1557T>G
20g.46016345A>GCA409228204MMP9,SLC12A5-AS1c.2101A>G (p.Ile701Val)
n.669-1557T>C
20g.46016345A>TCA409228206MMP9,SLC12A5-AS1c.2101A>T (p.Ile701Phe)
n.669-1557T>A
20g.46016346T>ACA409228220MMP9,SLC12A5-AS1c.2102T>A (p.Ile701Asn)
n.669-1558A>T
20g.46016346T>CCA409228215MMP9,SLC12A5-AS1c.2102T>C (p.Ile701Thr)
n.669-1558A>G
20g.46016346T>GCA409228210MMP9,SLC12A5-AS1c.2102T>G (p.Ile701Ser)
n.669-1558A>C
20g.46016347C>ACA510650773MMP9,SLC12A5-AS1c.2103C>A (p.Ile701=)
n.669-1559G>T
20g.46016347C>GCA409228263MMP9,SLC12A5-AS1c.2103C>G (p.Ile701Met)
n.669-1559G>C
20g.46016347C>TCA510650776MMP9,SLC12A5-AS1c.2103C>T (p.Ile701=)
n.669-1559G>A
20g.46016348C>ACA409228266MMP9,SLC12A5-AS1c.2104C>A (p.Leu702Met)
n.669-1560G>T
20g.46016348C=CA2366481091MMP9,SLC12A5-AS1c.2104C= (p.Leu702=)
n.669-1560G=

Number of alleles fetched