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.46373453A=CA1362082613CCR5,CCR5ASc.551A= (p.Tyr184=)
n.392-2036T=
3g.46373453A>CCA352471639CCR5,CCR5ASc.551A>C (p.Tyr184Ser)
n.392-2036T>G
3g.46373453A>GCA352471632CCR5,CCR5ASc.551A>G (p.Tyr184Cys)
n.392-2036T>C
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.46373453A>TCA352471637CCR5,CCR5ASc.551A>T (p.Tyr184Phe)
n.392-2036T>A
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.46373454C>ACA352471641CCR5,CCR5ASc.552C>A (p.Tyr184Ter)
n.392-2037G>T
3g.46373454C=CA1362082614CCR5,CCR5ASc.552C= (p.Tyr184=)
n.392-2037G=
3g.46373454C>GCA2354676CCR5,CCR5ASc.552C>G (p.Tyr184Ter)
n.392-2037G>C
dbSNP ExAC gnomAD v2 gnomAD v4
3g.46373454C>TCA73685268CCR5,CCR5ASc.552C>T (p.Tyr184=)
n.392-2037G>A
dbSNP
3g.46373455A=CA1362082615CCR5,CCR5ASc.553A= (p.Ser185=)
n.392-2038T=
3g.46373455A>CCA2354677CCR5,CCR5ASc.553A>C (p.Ser185Arg)
n.392-2038T>G
dbSNP ExAC gnomAD v2 gnomAD v4
3g.46373455A>GCA352471645CCR5,CCR5ASc.553A>G (p.Ser185Gly)
n.392-2038T>C
3g.46373455A>TCA352471647CCR5,CCR5ASc.553A>T (p.Ser185Cys)
n.392-2038T>A
3g.46373456G>ACA352471649CCR5,CCR5ASc.554G>A (p.Ser185Asn)
n.392-2039C>T
3g.46373456G>CCA352471651CCR5,CCR5ASc.554G>C (p.Ser185Thr)
n.392-2039C>G
3g.46373456G=CA1362082616CCR5,CCR5ASc.554G= (p.Ser185=)
n.392-2039C=
3g.46373456G>TCA73685282CCR5,CCR5ASc.554G>T (p.Ser185Ile)
n.392-2039C>A
dbSNP COSMIC
3g.46373457T>ACA352471654CCR5,CCR5ASc.555T>A (p.Ser185Arg)
n.392-2040A>T
3g.46373457T>CCA433593780CCR5,CCR5ASc.555T>C (p.Ser185=)
n.392-2040A>G
3g.46373457T>GCA73685290CCR5,CCR5ASc.555T>G (p.Ser185Arg)
n.392-2040A>C
dbSNP
3g.46373457T=CA1362082617CCR5,CCR5ASc.555T= (p.Ser185=)
n.392-2040A=
3g.46373458C>ACA73685292CCR5,CCR5ASc.556C>A (p.Gln186Lys)
n.392-2041G>T
dbSNP
3g.46373458C=CA1362082618CCR5,CCR5ASc.556C= (p.Gln186=)
n.392-2041G=
3g.46373458C>GCA352471658CCR5,CCR5ASc.556C>G (p.Gln186Glu)
n.392-2041G>C
3g.46373458C>TCA2354678CCR5,CCR5ASc.556C>T (p.Gln186Ter)
n.392-2041G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373459A>CCA352471661CCR5,CCR5ASc.557A>C (p.Gln186Pro)
n.392-2042T>G
3g.46373459A>GCA352471662CCR5,CCR5ASc.557A>G (p.Gln186Arg)
n.392-2042T>C
gnomAD v4
3g.46373459A>TCA352471663CCR5,CCR5ASc.557A>T (p.Gln186Leu)
n.392-2042T>A
3g.46373460G>ACA433593788CCR5,CCR5ASc.558G>A (p.Gln186=)
n.392-2043C>T
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
3g.46373460G>CCA352471665CCR5,CCR5ASc.558G>C (p.Gln186His)
n.392-2043C>G
3g.46373460G=CA1362082619CCR5,CCR5ASc.558G= (p.Gln186=)
n.392-2043C=
3g.46373460G>TCA352471666CCR5,CCR5ASc.558G>T (p.Gln186His)
n.392-2043C>A
3g.46373461T>ACA352471668CCR5,CCR5ASc.559T>A (p.Tyr187Asn)
n.392-2044A>T
3g.46373461T>CCA352471670CCR5,CCR5ASc.559T>C (p.Tyr187His)
n.392-2044A>G
3g.46373461T>GCA352471672CCR5,CCR5ASc.559T>G (p.Tyr187Asp)
n.392-2044A>C
3g.46373463_46373490delCA2577573859CCR5,CCR5ASc.561_588del (p.Tyr187Ter)
n.392-2071_392-2044del
3g.46373462A=CA1362082620CCR5,CCR5ASc.560A= (p.Tyr187=)
n.392-2045T=
3g.46373462A>CCA352471675CCR5,CCR5ASc.560A>C (p.Tyr187Ser)
n.392-2045T>G
3g.46373462A>GCA2354679CCR5,CCR5ASc.560A>G (p.Tyr187Cys)
n.392-2045T>C
dbSNP ExAC gnomAD v2
3g.46373462A>TCA352471678CCR5,CCR5ASc.560A>T (p.Tyr187Phe)
n.392-2045T>A
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

Number of alleles fetched