Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.46373485A>CCA352471828CCR5,CCR5ASc.583A>C (p.Thr195Pro)
n.392-2068T>G
3g.46373485A>GCA352471832CCR5,CCR5ASc.583A>G (p.Thr195Ala)
n.392-2068T>C
3g.46373485A>TCA352471834CCR5,CCR5ASc.583A>T (p.Thr195Ser)
n.392-2068T>A
3g.46373486C>ACA352471839CCR5,CCR5ASc.584C>A (p.Thr195Lys)
n.392-2069G>T
3g.46373486C=CA1362082632CCR5,CCR5ASc.584C= (p.Thr195=)
n.392-2069G=
3g.46373486C>GCA352471842CCR5,CCR5ASc.584C>G (p.Thr195Arg)
n.392-2069G>C
3g.46373486C>TCA2354686CCR5,CCR5ASc.584C>T (p.Thr195Ile)
n.392-2069G>A
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373487A=CA1362082633CCR5,CCR5ASc.585A= (p.Thr195=)
n.392-2070T=
3g.46373487A>CCA433593872CCR5,CCR5ASc.585A>C (p.Thr195=)
n.392-2070T>G
dbSNP
3g.46373487A>GCA433593874CCR5,CCR5ASc.585A>G (p.Thr195=)
n.392-2070T>C
3g.46373487A>TCA433593877CCR5,CCR5ASc.585A>T (p.Thr195=)
n.392-2070T>A
3g.46373488T>ACA352471850CCR5,CCR5ASc.586T>A (p.Leu196Ile)
n.392-2071A>T
3g.46373488T>CCA433593879CCR5,CCR5ASc.586T>C (p.Leu196=)
n.392-2071A>G
3g.46373488T>GCA352471854CCR5,CCR5ASc.586T>G (p.Leu196Val)
n.392-2071A>C
3g.46373489T>ACA352471864CCR5,CCR5ASc.587T>A (p.Leu196Ter)
n.392-2072A>T
3g.46373489T>CCA352471859CCR5,CCR5ASc.587T>C (p.Leu196Ser)
n.392-2072A>G
3g.46373489T>GCA352471862CCR5,CCR5ASc.587T>G (p.Leu196Ter)
n.392-2072A>C
3g.46373490A>CCA352471865CCR5,CCR5ASc.588A>C (p.Leu196Phe)
n.392-2073T>G
3g.46373490A>GCA433593887CCR5,CCR5ASc.588A>G (p.Leu196=)
n.392-2073T>C
3g.46373490A>TCA352471866CCR5,CCR5ASc.588A>T (p.Leu196Phe)
n.392-2073T>A
3g.46373491A>CCA352471867CCR5,CCR5ASc.589A>C (p.Lys197Gln)
n.392-2074T>G
3g.46373491A>GCA352471868CCR5,CCR5ASc.589A>G (p.Lys197Glu)
n.392-2074T>C
3g.46373491A>TCA352471869CCR5,CCR5ASc.589A>T (p.Lys197Ter)
n.392-2074T>A
3g.46373492A>CCA352471870CCR5,CCR5ASc.590A>C (p.Lys197Thr)
n.392-2075T>G
3g.46373492A>GCA352471871CCR5,CCR5ASc.590A>G (p.Lys197Arg)
n.392-2075T>C
3g.46373492A>TCA352471872CCR5,CCR5ASc.590A>T (p.Lys197Met)
n.392-2075T>A
3g.46373493G>ACA2354687CCR5,CCR5ASc.591G>A (p.Lys197=)
n.392-2076C>T
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.46373493G>CCA352471876CCR5,CCR5ASc.591G>C (p.Lys197Asn)
n.392-2076C>G
3g.46373493G=CA1362082634CCR5,CCR5ASc.591G= (p.Lys197=)
n.392-2076C=
3g.46373493G>TCA352471879CCR5,CCR5ASc.591G>T (p.Lys197Asn)
n.392-2076C>A
dbSNP gnomAD v3 gnomAD v4
3g.46373494A>CCA352471891CCR5,CCR5ASc.592A>C (p.Ile198Leu)
n.392-2077T>G
3g.46373494A>GCA352471885CCR5,CCR5ASc.592A>G (p.Ile198Val)
n.392-2077T>C
COSMIC
3g.46373494A>TCA352471889CCR5,CCR5ASc.592A>T (p.Ile198Leu)
n.392-2077T>A
3g.46373495T>ACA352471893CCR5,CCR5ASc.593T>A (p.Ile198Lys)
n.392-2078A>T
3g.46373495T>CCA352471900CCR5,CCR5ASc.593T>C (p.Ile198Thr)
n.392-2078A>G
3g.46373495T>GCA352471898CCR5,CCR5ASc.593T>G (p.Ile198Arg)
n.392-2078A>C
3g.46373496A>CCA433593904CCR5,CCR5ASc.594A>C (p.Ile198=)
n.392-2079T>G
3g.46373496A>GCA352471905CCR5,CCR5ASc.594A>G (p.Ile198Met)
n.392-2079T>C
3g.46373496A>TCA433593906CCR5,CCR5ASc.594A>T (p.Ile198=)
n.392-2079T>A
3g.46373497G>ACA73685345CCR5,CCR5ASc.595G>A (p.Val199Ile)
n.392-2080C>T
dbSNP
3g.46373497G>CCA352471957CCR5,CCR5ASc.595G>C (p.Val199Leu)
n.392-2080C>G
gnomAD v4
3g.46373497G=CA1362082635CCR5,CCR5ASc.595G= (p.Val199=)
n.392-2080C=
3g.46373497G>TCA352471961CCR5,CCR5ASc.595G>T (p.Val199Phe)
n.392-2080C>A
3g.46373498T>ACA352471968CCR5,CCR5ASc.596T>A (p.Val199Asp)
n.392-2081A>T
dbSNP
3g.46373498T>CCA352471971CCR5,CCR5ASc.596T>C (p.Val199Ala)
n.392-2081A>G
dbSNP gnomAD v2 gnomAD v4
3g.46373498T>GCA352471974CCR5,CCR5ASc.596T>G (p.Val199Gly)
n.392-2081A>C
3g.46373498T=CA1362082636CCR5,CCR5ASc.596T= (p.Val199=)
n.392-2081A=

Number of alleles fetched