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.46373463T>ACA352471679CCR5,CCR5ASc.561T>A (p.Tyr187Ter)
n.392-2046A>T
gnomAD v4
3g.46373463T>CCA433593796CCR5,CCR5ASc.561T>C (p.Tyr187=)
n.392-2046A>G
dbSNP
3g.46373463T>GCA352471681CCR5,CCR5ASc.561T>G (p.Tyr187Ter)
n.392-2046A>C
3g.46373463T=CA1362082621CCR5,CCR5ASc.561T= (p.Tyr187=)
n.392-2046A=
3g.46373464C>ACA352471686CCR5,CCR5ASc.562C>A (p.Gln188Lys)
n.392-2047G>T
3g.46373464C>GCA352471684CCR5,CCR5ASc.562C>G (p.Gln188Glu)
n.392-2047G>C
3g.46373464C>TCA352471682CCR5,CCR5ASc.562C>T (p.Gln188Ter)
n.392-2047G>A
gnomAD v4
3g.46373465A>CCA352471688CCR5,CCR5ASc.563A>C (p.Gln188Pro)
n.392-2048T>G
3g.46373465A>GCA352471690CCR5,CCR5ASc.563A>G (p.Gln188Arg)
n.392-2048T>C
3g.46373465A>TCA352471691CCR5,CCR5ASc.563A>T (p.Gln188Leu)
n.392-2048T>A
3g.46373466A>CCA352471693CCR5,CCR5ASc.564A>C (p.Gln188His)
n.392-2049T>G
3g.46373466A>GCA433593808CCR5,CCR5ASc.564A>G (p.Gln188=)
n.392-2049T>C
gnomAD v4
3g.46373466A>TCA352471695CCR5,CCR5ASc.564A>T (p.Gln188His)
n.392-2049T>A
3g.46373467T>ACA2354681CCR5,CCR5ASc.565T>A (p.Phe189Ile)
n.392-2050A>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373467T>CCA2354680CCR5,CCR5ASc.565T>C (p.Phe189Leu)
n.392-2050A>G
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373467T>GCA352471697CCR5,CCR5ASc.565T>G (p.Phe189Val)
n.392-2050A>C
3g.46373467T=CA1362082622CCR5,CCR5ASc.565T= (p.Phe189=)
n.392-2050A=
3g.46373468T>ACA352471699CCR5,CCR5ASc.566T>A (p.Phe189Tyr)
n.392-2051A>T
3g.46373468T>CCA352471701CCR5,CCR5ASc.566T>C (p.Phe189Ser)
n.392-2051A>G
gnomAD v4
3g.46373468T>GCA352471703CCR5,CCR5ASc.566T>G (p.Phe189Cys)
n.392-2051A>C
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

Number of alleles fetched