Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.46373452_46373484delinsTACAGTCAGTATCAATTCTGGAAGAATTTCCAGCA1362082611CCR5,CCR5ASc.550_582delinsTACAGTCAGTATCAATTCTGGAAGAATTTCCAG (p.Tyr184=)
n.392-2067_392-2035delinsCTGGAAATTCTTCCAGAATTGATACTGACTGTA
3g.46373452_46373513delCA2665436444CCR5,CCR5ASc.550_611del (p.Tyr184ProfsTer23)
n.392-2096_392-2035del
gnomAD v4
3g.46373456_46373487delCA119355CCR5,CCR5ASc.554_585del (p.Ser185IlefsTer?)
n.392-2067_392-2036del
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.46373463_46373490delCA2577573859CCR5,CCR5ASc.561_588del (p.Tyr187Ter)
n.392-2071_392-2044del
3g.46373469C>ACA352471705CCR5,CCR5ASc.567C>A (p.Phe189Leu)
n.392-2052G>T
3g.46373469C=CA1362082623CCR5,CCR5ASc.567C= (p.Phe189=)
n.392-2052G=
3g.46373469C>GCA352471706CCR5,CCR5ASc.567C>G (p.Phe189Leu)
n.392-2052G>C
dbSNP gnomAD v4
3g.46373469C>TCA433593814CCR5,CCR5ASc.567C>T (p.Phe189=)
n.392-2052G>A
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.46373470T>ACA352471711CCR5,CCR5ASc.568T>A (p.Trp190Arg)
n.392-2053A>T
3g.46373470T>CCA2354682CCR5,CCR5ASc.568T>C (p.Trp190Arg)
n.392-2053A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373470T>GCA2354683CCR5,CCR5ASc.568T>G (p.Trp190Gly)
n.392-2053A>C
dbSNP ExAC gnomAD v2 gnomAD v4
3g.46373470T=CA1362082624CCR5,CCR5ASc.568T= (p.Trp190=)
n.392-2053A=
3g.46373471G>ACA352471716CCR5,CCR5ASc.569G>A (p.Trp190Ter)
n.392-2054C>T
dbSNP gnomAD v3 gnomAD v4
3g.46373471G>CCA352471719CCR5,CCR5ASc.569G>C (p.Trp190Ser)
n.392-2054C>G
3g.46373471G=CA1362082625CCR5,CCR5ASc.569G= (p.Trp190=)
n.392-2054C=
3g.46373471G>TCA352471721CCR5,CCR5ASc.569G>T (p.Trp190Leu)
n.392-2054C>A
3g.46373472delCA2665436445CCR5,CCR5ASc.570del (p.Trp190Ter)
n.392-2054del
gnomAD v4
3g.46373472G>ACA352471726CCR5,CCR5ASc.570G>A (p.Trp190Ter)
n.392-2055C>T
3g.46373472G>CCA352471729CCR5,CCR5ASc.570G>C (p.Trp190Cys)
n.392-2055C>G
gnomAD v4
3g.46373472G=CA1362082626CCR5,CCR5ASc.570G= (p.Trp190=)
n.392-2055C=
3g.46373472G>TCA2354684CCR5,CCR5ASc.570G>T (p.Trp190Cys)
n.392-2055C>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373473A>CCA352471738CCR5,CCR5ASc.571A>C (p.Lys191Gln)
n.392-2056T>G
3g.46373473A>GCA352471734CCR5,CCR5ASc.571A>G (p.Lys191Glu)
n.392-2056T>C
3g.46373473A>TCA352471737CCR5,CCR5ASc.571A>T (p.Lys191Ter)
n.392-2056T>A
3g.46373474A>CCA352471743CCR5,CCR5ASc.572A>C (p.Lys191Thr)
n.392-2057T>G
3g.46373474A>GCA352471746CCR5,CCR5ASc.572A>G (p.Lys191Arg)
n.392-2057T>C
3g.46373474A>TCA352471748CCR5,CCR5ASc.572A>T (p.Lys191Met)
n.392-2057T>A
3g.46373475G>ACA433593827CCR5,CCR5ASc.573G>A (p.Lys191=)
n.392-2058C>T
gnomAD v4
3g.46373475G>CCA352471752CCR5,CCR5ASc.573G>C (p.Lys191Asn)
n.392-2058C>G
COSMIC
3g.46373475G>TCA352471755CCR5,CCR5ASc.573G>T (p.Lys191Asn)
n.392-2058C>A
3g.46373476A>CCA352471763CCR5,CCR5ASc.574A>C (p.Asn192His)
n.392-2059T>G
3g.46373476A>GCA352471758CCR5,CCR5ASc.574A>G (p.Asn192Asp)
n.392-2059T>C
3g.46373476A>TCA352471761CCR5,CCR5ASc.574A>T (p.Asn192Tyr)
n.392-2059T>A
3g.46373477A=CA1362082627CCR5,CCR5ASc.575A= (p.Asn192=)
n.392-2060T=
3g.46373477A>CCA352471768CCR5,CCR5ASc.575A>C (p.Asn192Thr)
n.392-2060T>G
3g.46373477A>GCA352471770CCR5,CCR5ASc.575A>G (p.Asn192Ser)
n.392-2060T>C
3g.46373477A>TCA73685316CCR5,CCR5ASc.575A>T (p.Asn192Ile)
n.392-2060T>A
dbSNP
3g.46373478T>ACA352471776CCR5,CCR5ASc.576T>A (p.Asn192Lys)
n.392-2061A>T
3g.46373478T>CCA433593833CCR5,CCR5ASc.576T>C (p.Asn192=)
n.392-2061A>G
3g.46373478T>GCA352471777CCR5,CCR5ASc.576T>G (p.Asn192Lys)
n.392-2061A>C
3g.46373479T>ACA352471780CCR5,CCR5ASc.577T>A (p.Phe193Ile)
n.392-2062A>T
3g.46373479T>CCA352471782CCR5,CCR5ASc.577T>C (p.Phe193Leu)
n.392-2062A>G
gnomAD v4
3g.46373479T>GCA352471783CCR5,CCR5ASc.577T>G (p.Phe193Val)
n.392-2062A>C
3g.46373480T>ACA352471786CCR5,CCR5ASc.578T>A (p.Phe193Tyr)
n.392-2063A>T
3g.46373480T>CCA73685319CCR5,CCR5ASc.578T>C (p.Phe193Ser)
n.392-2063A>G
dbSNP gnomAD v4
3g.46373480T>GCA352471790CCR5,CCR5ASc.578T>G (p.Phe193Cys)
n.392-2063A>C
3g.46373480T=CA1362082628CCR5,CCR5ASc.578T= (p.Phe193=)
n.392-2063A=
3g.46373481C>ACA352471794CCR5,CCR5ASc.579C>A (p.Phe193Leu)
n.392-2064G>T
3g.46373481C=CA1362082629CCR5,CCR5ASc.579C= (p.Phe193=)
n.392-2064G=
3g.46373481C>GCA2354685CCR5,CCR5ASc.579C>G (p.Phe193Leu)
n.392-2064G>C
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched