Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.39265665G>ACA352200159CX3CR1c.845C>T (p.Ala282Val)
c.941C>T (p.Ala314Val)
3g.39265665G>CCA352200161CX3CR1c.845C>G (p.Ala282Gly)
c.941C>G (p.Ala314Gly)
3g.39265665G>TCA352200163CX3CR1c.845C>A (p.Ala282Glu)
c.941C>A (p.Ala314Glu)
3g.39265665dupCA542616777CX3CR1c.845dup (p.Phe283IlefsTer2)
c.941dup (p.Phe315IlefsTer2)
dbSNP gnomAD
3g.39265666C>ACA352200166CX3CR1c.844G>T (p.Ala282Ser)
c.940G>T (p.Ala314Ser)
3g.39265666C>GCA352200167CX3CR1c.844G>C (p.Ala282Pro)
c.940G>C (p.Ala314Pro)
3g.39265666C>TCA352200168CX3CR1c.844G>A (p.Ala282Thr)
c.940G>A (p.Ala314Thr)
3g.39265667A>CCA433147874CX3CR1c.843T>G (p.Val281=)
c.939T>G (p.Val313=)
3g.39265667A>GCA433147877CX3CR1c.843T>C (p.Val281=)
c.939T>C (p.Val313=)
3g.39265667A>TCA433147879CX3CR1c.843T>A (p.Val281=)
c.939T>A (p.Val313=)
3g.39265668A>CCA352200169CX3CR1c.842T>G (p.Val281Gly)
c.938T>G (p.Val313Gly)
3g.39265668A>GCA2326890CX3CR1c.842T>C (p.Val281Ala)
c.938T>C (p.Val313Ala)
dbSNP ExAC gnomAD
3g.39265668A>TCA352200173CX3CR1c.842T>A (p.Val281Asp)
c.938T>A (p.Val313Asp)
3g.39265669C>ACA352200187CX3CR1c.841G>T (p.Val281Phe)
c.937G>T (p.Val313Phe)
COSMIC COSMIC
3g.39265669C>GCA352200190CX3CR1c.841G>C (p.Val281Leu)
c.937G>C (p.Val313Leu)
3g.39265669C>TCA352200184CX3CR1c.841G>A (p.Val281Ile)
c.937G>A (p.Val313Ile)
3g.39265670C>ACA433341724CX3CR1c.840G>T (p.Thr280=)
c.936G>T (p.Thr312=)
COSMIC COSMIC
3g.39265670C>GCA433341725CX3CR1c.840G>C (p.Thr280=)
c.936G>C (p.Thr312=)
3g.39265670C>TCA73027630CX3CR1c.840G>A (p.Thr280=)
c.936G>A (p.Thr312=)
dbSNP gnomAD COSMIC COSMIC
3g.39265671G>ACA031130CX3CR1c.839C>T (p.Thr280Met)
c.935C>T (p.Thr312Met)
dbSNP ExAC gnomAD
3g.[39265671G>A;39265765C>T]CA031269CX3CR1c.[745G>A;839C>T] (p.[Val249Ile;Thr280Met])
c.[841G>A;935C>T] (p.[Val281Ile;Thr312Met])
ClinVar
3g.39265671G>CCA352200193CX3CR1c.839C>G (p.Thr280Arg)
c.935C>G (p.Thr312Arg)
3g.39265671G>TCA352200194CX3CR1c.839C>A (p.Thr280Lys)
c.935C>A (p.Thr312Lys)
3g.39265672T>ACA352200195CX3CR1c.838A>T (p.Thr280Ser)
c.934A>T (p.Thr312Ser)
3g.39265672T>CCA2326891CX3CR1c.838A>G (p.Thr280Ala)
c.934A>G (p.Thr312Ala)
dbSNP ExAC gnomAD
3g.39265672T>GCA352200197CX3CR1c.838A>C (p.Thr280Pro)
c.934A>C (p.Thr312Pro)
3g.39265673C>ACA352200199CX3CR1c.837G>T (p.Glu279Asp)
c.933G>T (p.Glu311Asp)
3g.39265673C>GCA352200202CX3CR1c.837G>C (p.Glu279Asp)
c.933G>C (p.Glu311Asp)
3g.39265673C>TCA433341727CX3CR1c.837G>A (p.Glu279=)
c.933G>A (p.Glu311=)
3g.39265674T>ACA352200206CX3CR1c.836A>T (p.Glu279Val)
c.932A>T (p.Glu311Val)
3g.39265674T>CCA2326892CX3CR1c.836A>G (p.Glu279Gly)
c.932A>G (p.Glu311Gly)
dbSNP ExAC gnomAD
3g.39265674T>GCA352200208CX3CR1c.836A>C (p.Glu279Ala)
c.932A>C (p.Glu311Ala)
3g.39265675C>ACA352200212CX3CR1c.835G>T (p.Glu279Ter)
c.931G>T (p.Glu311Ter)
3g.39265675C>GCA352200223CX3CR1c.835G>C (p.Glu279Gln)
c.931G>C (p.Glu311Gln)
COSMIC COSMIC
3g.39265675C>TCA352200210CX3CR1c.835G>A (p.Glu279Lys)
c.931G>A (p.Glu311Lys)
COSMIC COSMIC
3g.39265676A>CCA433341729CX3CR1c.834T>G (p.Thr278=)
c.930T>G (p.Thr310=)
3g.39265676A>GCA433341730CX3CR1c.834T>C (p.Thr278=)
c.930T>C (p.Thr310=)
3g.39265676A>TCA433341731CX3CR1c.834T>A (p.Thr278=)
c.930T>A (p.Thr310=)
3g.39265677G>ACA352200224CX3CR1c.833C>T (p.Thr278Ile)
c.929C>T (p.Thr310Ile)
3g.39265677G>CCA352200225CX3CR1c.833C>G (p.Thr278Ser)
c.929C>G (p.Thr310Ser)
3g.39265677G>TCA352200226CX3CR1c.833C>A (p.Thr278Asn)
c.929C>A (p.Thr310Asn)
3g.39265678T>ACA352200228CX3CR1c.832A>T (p.Thr278Ser)
c.928A>T (p.Thr310Ser)
3g.39265678T>CCA2326893CX3CR1c.832A>G (p.Thr278Ala)
c.928A>G (p.Thr310Ala)
dbSNP ExAC gnomAD
3g.39265678T>GCA352200244CX3CR1c.832A>C (p.Thr278Pro)
c.928A>C (p.Thr310Pro)
3g.39265679C>ACA433341735CX3CR1c.831G>T (p.Val277=)
c.927G>T (p.Val309=)
3g.39265679C>GCA433341736CX3CR1c.831G>C (p.Val277=)
c.927G>C (p.Val309=)
3g.39265679C>TCA433341737CX3CR1c.831G>A (p.Val277=)
c.927G>A (p.Val309=)
COSMIC COSMIC
3g.39265680A>CCA352200249CX3CR1c.830T>G (p.Val277Gly)
c.926T>G (p.Val309Gly)
3g.39265680A>GCA352200247CX3CR1c.830T>C (p.Val277Ala)
c.926T>C (p.Val309Ala)
3g.39265680A>TCA352200248CX3CR1c.830T>A (p.Val277Glu)
c.926T>A (p.Val309Glu)

Number of alleles fetched