Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.39265580T>ACA352199575CX3CR1c.930A>T (p.Lys310Asn)
c.1026A>T (p.Lys342Asn)
3g.39265580T>CCA433147546CX3CR1c.930A>G (p.Lys310=)
c.1026A>G (p.Lys342=)
3g.39265580T>GCA352199576CX3CR1c.930A>C (p.Lys310Asn)
c.1026A>C (p.Lys342Asn)
3g.39265581T>ACA352199578CX3CR1c.929A>T (p.Lys310Ile)
c.1025A>T (p.Lys342Ile)
COSMIC COSMIC
3g.39265581T>CCA352199582CX3CR1c.929A>G (p.Lys310Arg)
c.1025A>G (p.Lys342Arg)
3g.39265581T>GCA352199585CX3CR1c.929A>C (p.Lys310Thr)
c.1025A>C (p.Lys342Thr)
3g.39265582T>ACA352199587CX3CR1c.928A>T (p.Lys310Ter)
c.1024A>T (p.Lys342Ter)
3g.39265582T>CCA352199590CX3CR1c.928A>G (p.Lys310Glu)
c.1024A>G (p.Lys342Glu)
3g.39265582T>GCA352199593CX3CR1c.928A>C (p.Lys310Gln)
c.1024A>C (p.Lys342Gln)
dbSNP
3g.39265582T=CA1358882776CX3CR1c.928A= (p.Lys310=)
c.1024A= (p.Lys342=)
3g.39265582_39265583delinsTCCA1358882777CX3CR1c.927_928delinsGA (p.Gly309=)
c.1023_1024delinsGA (p.Gly341=)
3g.39265583C>ACA433147557CX3CR1c.927G>T (p.Gly309=)
c.1023G>T (p.Gly341=)
3g.39265583C>GCA433147559CX3CR1c.927G>C (p.Gly309=)
c.1023G>C (p.Gly341=)
COSMIC COSMIC
3g.39265583C>TCA433147560CX3CR1c.927G>A (p.Gly309=)
c.1023G>A (p.Gly341=)
COSMIC COSMIC
3g.39265585delCA1358882778CX3CR1c.927del (p.Lys310AsnfsTer29)
c.1023del (p.Lys342AsnfsTer29)
dbSNP
3g.39265584C>ACA352199598CX3CR1c.926G>T (p.Gly309Val)
c.1022G>T (p.Gly341Val)
3g.39265584C>GCA352199609CX3CR1c.926G>C (p.Gly309Ala)
c.1022G>C (p.Gly341Ala)
3g.39265584C>TCA352199610CX3CR1c.926G>A (p.Gly309Glu)
c.1022G>A (p.Gly341Glu)
gnomAD v4
3g.39265585C>ACA352199613CX3CR1c.925G>T (p.Gly309Trp)
c.1021G>T (p.Gly341Trp)
COSMIC COSMIC
3g.39265585C=CA1358882779CX3CR1c.925G= (p.Gly309=)
c.1021G= (p.Gly341=)
3g.39265585C>GCA352199611CX3CR1c.925G>C (p.Gly309Arg)
c.1021G>C (p.Gly341Arg)
3g.39265585C>TCA352199612CX3CR1c.925G>A (p.Gly309Arg)
c.1021G>A (p.Gly341Arg)
dbSNP
3g.39265586A=CA1358882780CX3CR1c.924T= (p.Tyr308=)
c.1020T= (p.Tyr340=)
3g.39265586A>CCA352199616CX3CR1c.924T>G (p.Tyr308Ter)
c.1020T>G (p.Tyr340Ter)
3g.39265586A>GCA433147572CX3CR1c.924T>C (p.Tyr308=)
c.1020T>C (p.Tyr340=)
dbSNP gnomAD v2 gnomAD v4
3g.39265586A>TCA352199618CX3CR1c.924T>A (p.Tyr308Ter)
c.1020T>A (p.Tyr340Ter)
3g.39265587T>ACA352199624CX3CR1c.923A>T (p.Tyr308Phe)
c.1019A>T (p.Tyr340Phe)
3g.39265587T>CCA352199626CX3CR1c.923A>G (p.Tyr308Cys)
c.1019A>G (p.Tyr340Cys)
gnomAD v4
3g.39265587T>GCA352199627CX3CR1c.923A>C (p.Tyr308Ser)
c.1019A>C (p.Tyr340Ser)
3g.39265588A=CA1358882781CX3CR1c.922T= (p.Tyr308=)
c.1018T= (p.Tyr340=)
3g.39265588A>CCA352199631CX3CR1c.922T>G (p.Tyr308Asp)
c.1018T>G (p.Tyr340Asp)
3g.39265588A>GCA352199632CX3CR1c.922T>C (p.Tyr308His)
c.1018T>C (p.Tyr340His)
dbSNP gnomAD v3 gnomAD v4
3g.39265588A>TCA352199634CX3CR1c.922T>A (p.Tyr308Asn)
c.1018T>A (p.Tyr340Asn)
3g.39265589C>ACA433147583CX3CR1c.921G>T (p.Leu307=)
c.1017G>T (p.Leu339=)
gnomAD v4
3g.39265589C>GCA433147585CX3CR1c.921G>C (p.Leu307=)
c.1017G>C (p.Leu339=)
3g.39265589C>TCA433147586CX3CR1c.921G>A (p.Leu307=)
c.1017G>A (p.Leu339=)
3g.39265590A>CCA352199637CX3CR1c.920T>G (p.Leu307Arg)
c.1016T>G (p.Leu339Arg)
3g.39265590A>GCA352199640CX3CR1c.920T>C (p.Leu307Pro)
c.1016T>C (p.Leu339Pro)
gnomAD v4
3g.39265590A>TCA352199642CX3CR1c.920T>A (p.Leu307Gln)
c.1016T>A (p.Leu339Gln)
3g.39265591G>ACA433147590CX3CR1c.919C>T (p.Leu307=)
c.1015C>T (p.Leu339=)
gnomAD v4
3g.39265591G>CCA352199650CX3CR1c.919C>G (p.Leu307Val)
c.1015C>G (p.Leu339Val)
3g.39265591G>TCA352199646CX3CR1c.919C>A (p.Leu307Met)
c.1015C>A (p.Leu339Met)
3g.39265592G>ACA433147593CX3CR1c.918C>T (p.His306=)
c.1014C>T (p.His338=)
gnomAD v4
3g.39265592G>CCA352199653CX3CR1c.918C>G (p.His306Gln)
c.1014C>G (p.His338Gln)
3g.39265592G>TCA352199654CX3CR1c.918C>A (p.His306Gln)
c.1014C>A (p.His338Gln)
3g.39265593T>ACA352199657CX3CR1c.917A>T (p.His306Leu)
c.1013A>T (p.His338Leu)
3g.39265593T>CCA352199660CX3CR1c.917A>G (p.His306Arg)
c.1013A>G (p.His338Arg)
3g.39265593T>GCA352199663CX3CR1c.917A>C (p.His306Pro)
c.1013A>C (p.His338Pro)
3g.39265594G>ACA352199664CX3CR1c.916C>T (p.His306Tyr)
c.1012C>T (p.His338Tyr)
dbSNP gnomAD v2 gnomAD v4
3g.39265594G>CCA352199665CX3CR1c.916C>G (p.His306Asp)
c.1012C>G (p.His338Asp)

Number of alleles fetched