Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.159205719_159205738delinsCCTGGCTGGCCTGTCCTGGCCA1148224757ACKR1c.286_305delinsCCTGGCTGGCCTGTCCTGGC (p.Pro96=)
c.280_299delinsCCTGGCTGGCCTGTCCTGGC (p.Pro94=)
n.461_480delinsCCTGGCTGGCCTGTCCTGGC
1g.159205725_159205738delCA113791ACKR1c.292_305del (p.Trp98ThrfsTer22)
c.286_299del (p.Trp96ThrfsTer22)
n.467_480del
ClinVar dbSNP gnomAD v4
1g.159205737G>ACA1187699ACKR1c.304G>A (p.Ala102Thr)
c.298G>A (p.Ala100Thr)
n.479G>A
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.159205737G>CCA343057775ACKR1c.304G>C (p.Ala102Pro)
c.298G>C (p.Ala100Pro)
n.479G>C
1g.159205737G=CA1139774015ACKR1c.304G= (p.Ala102=)
c.298G= (p.Ala100=)
n.479G=
1g.159205737G>TCA343057774ACKR1c.304G>T (p.Ala102Ser)
c.298G>T (p.Ala100Ser)
n.479G>T
gnomAD v4
1g.159205738C>ACA343057776ACKR1c.305C>A (p.Ala102Glu)
c.299C>A (p.Ala100Glu)
n.480C>A
dbSNP gnomAD v2 gnomAD v4
1g.159205738C=CA1143928846ACKR1c.305C= (p.Ala102=)
c.299C= (p.Ala100=)
n.480C=
1g.159205738C>GCA343057777ACKR1c.305C>G (p.Ala102Gly)
c.299C>G (p.Ala100Gly)
n.480C>G
1g.159205738C>TCA1187700ACKR1c.305C>T (p.Ala102Val)
c.299C>T (p.Ala100Val)
n.480C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.159205739A>CCA421592987ACKR1c.306A>C (p.Ala102=)
c.300A>C (p.Ala100=)
n.481A>C
1g.159205739A>GCA421592988ACKR1c.306A>G (p.Ala102=)
c.300A>G (p.Ala100=)
n.481A>G
1g.159205739A>TCA421592990ACKR1c.306A>T (p.Ala102=)
c.300A>T (p.Ala100=)
n.481A>T
1g.159205740C>ACA343057778ACKR1c.307C>A (p.Gln103Lys)
c.301C>A (p.Gln101Lys)
n.482C>A
gnomAD v4 COSMIC
1g.159205740C>GCA343057779ACKR1c.307C>G (p.Gln103Glu)
c.301C>G (p.Gln101Glu)
n.482C>G
gnomAD v4
1g.159205740C>TCA343057780ACKR1c.307C>T (p.Gln103Ter)
c.301C>T (p.Gln101Ter)
n.482C>T
gnomAD v4
1g.159205741A>CCA343057781ACKR1c.308A>C (p.Gln103Pro)
c.302A>C (p.Gln101Pro)
n.483A>C
1g.159205741A>GCA343057782ACKR1c.308A>G (p.Gln103Arg)
c.302A>G (p.Gln101Arg)
n.483A>G
1g.159205741A>TCA343057783ACKR1c.308A>T (p.Gln103Leu)
c.302A>T (p.Gln101Leu)
n.483A>T
1g.159205742G>ACA421592992ACKR1c.309G>A (p.Gln103=)
c.303G>A (p.Gln101=)
n.484G>A
dbSNP gnomAD v2 gnomAD v4
1g.159205742G>CCA343057784ACKR1c.309G>C (p.Gln103His)
c.303G>C (p.Gln101His)
n.484G>C
1g.159205742G=CA1201790339ACKR1c.309G= (p.Gln103=)
c.303G= (p.Gln101=)
n.484G=
1g.159205742G>TCA343057785ACKR1c.309G>T (p.Gln103His)
c.303G>T (p.Gln101His)
n.484G>T
gnomAD v4
1g.159205743C>ACA343057786ACKR1c.310C>A (p.Leu104Met)
c.304C>A (p.Leu102Met)
n.485C>A
1g.159205743C>GCA343057787ACKR1c.310C>G (p.Leu104Val)
c.304C>G (p.Leu102Val)
n.485C>G
1g.159205743C>TCA421592994ACKR1c.310C>T (p.Leu104=)
c.304C>T (p.Leu102=)
n.485C>T
1g.159205744T>ACA343057790ACKR1c.311T>A (p.Leu104Gln)
c.305T>A (p.Leu102Gln)
n.486T>A
1g.159205744T>CCA343057789ACKR1c.311T>C (p.Leu104Pro)
c.305T>C (p.Leu102Pro)
n.486T>C
1g.159205744T>GCA343057788ACKR1c.311T>G (p.Leu104Arg)
c.305T>G (p.Leu102Arg)
n.486T>G
1g.159205745G>ACA421592995ACKR1c.312G>A (p.Leu104=)
c.306G>A (p.Leu102=)
n.487G>A
1g.159205745G>CCA421592996ACKR1c.312G>C (p.Leu104=)
c.306G>C (p.Leu102=)
n.487G>C
1g.159205745G>TCA421592997ACKR1c.312G>T (p.Leu104=)
c.306G>T (p.Leu102=)
n.487G>T
1g.159205746G>ACA343057791ACKR1c.313G>A (p.Ala105Thr)
c.307G>A (p.Ala103Thr)
n.488G>A
1g.159205746G>CCA343057792ACKR1c.313G>C (p.Ala105Pro)
c.307G>C (p.Ala103Pro)
n.488G>C
dbSNP gnomAD v3 gnomAD v4
1g.159205746G=CA1201790340ACKR1c.313G= (p.Ala105=)
c.307G= (p.Ala103=)
n.488G=
1g.159205746G>TCA343057793ACKR1c.313G>T (p.Ala105Ser)
c.307G>T (p.Ala103Ser)
n.488G>T
gnomAD v4
1g.159205747C>ACA343057794ACKR1c.314C>A (p.Ala105Asp)
c.308C>A (p.Ala103Asp)
n.489C>A
1g.159205747C>GCA343057795ACKR1c.314C>G (p.Ala105Gly)
c.308C>G (p.Ala103Gly)
n.489C>G
1g.159205747C>TCA343057796ACKR1c.314C>T (p.Ala105Val)
c.308C>T (p.Ala103Val)
n.489C>T
COSMIC COSMIC
1g.159205748T>ACA31347157ACKR1c.315T>A (p.Ala105=)
c.309T>A (p.Ala103=)
n.490T>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.159205748T>CCA421593000ACKR1c.315T>C (p.Ala105=)
c.309T>C (p.Ala103=)
n.490T>C
1g.159205748T>GCA421593001ACKR1c.315T>G (p.Ala105=)
c.309T>G (p.Ala103=)
n.490T>G
1g.159205748T=CA1142252426ACKR1c.315T= (p.Ala105=)
c.309T= (p.Ala103=)
n.490T=
1g.159205749G>ACA1187701ACKR1c.316G>A (p.Val106Met)
c.310G>A (p.Val104Met)
n.491G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.159205749G>CCA343057797ACKR1c.316G>C (p.Val106Leu)
c.310G>C (p.Val104Leu)
n.491G>C
1g.159205749G=CA1201790341ACKR1c.316G= (p.Val106=)
c.310G= (p.Val104=)
n.491G=
1g.159205749G>TCA343057798ACKR1c.316G>T (p.Val106Leu)
c.310G>T (p.Val104Leu)
n.491G>T
gnomAD v4
1g.159205750T>ACA343057799ACKR1c.317T>A (p.Val106Glu)
c.311T>A (p.Val104Glu)
n.492T>A
COSMIC
1g.159205750T>CCA1187702ACKR1c.317T>C (p.Val106Ala)
c.311T>C (p.Val104Ala)
n.492T>C
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.159205750T>GCA343057800ACKR1c.317T>G (p.Val106Gly)
c.311T>G (p.Val104Gly)
n.492T>G

Number of alleles fetched