Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.46373187C>ACA352469673CCR5,CCR5ASc.285C>A (p.Asp95Glu)
n.392-1770G>T
3g.46373187C>GCA352469674CCR5,CCR5ASc.285C>G (p.Asp95Glu)
n.392-1770G>C
3g.46373187C>TCA433593696CCR5,CCR5ASc.285C>T (p.Asp95=)
n.392-1770G>A
3g.46373188T>ACA352469677CCR5,CCR5ASc.286T>A (p.Phe96Ile)
n.392-1771A>T
3g.46373188T>CCA2354606CCR5,CCR5ASc.286T>C (p.Phe96Leu)
n.392-1771A>G
dbSNP ExAC gnomAD v2 gnomAD v4
3g.46373188T>GCA352469678CCR5,CCR5ASc.286T>G (p.Phe96Val)
n.392-1771A>C
3g.46373188T=CA1362082478CCR5,CCR5ASc.286T= (p.Phe96=)
n.392-1771A=
3g.46373190delCA2665436253CCR5,CCR5ASc.288del (p.Phe96LeufsTer9)
n.392-1771del
gnomAD v4
3g.46373189T>ACA352469680CCR5,CCR5ASc.287T>A (p.Phe96Tyr)
n.392-1772A>T
3g.46373189T>CCA352469681CCR5,CCR5ASc.287T>C (p.Phe96Ser)
n.392-1772A>G
3g.46373189T>GCA352469683CCR5,CCR5ASc.287T>G (p.Phe96Cys)
n.392-1772A>C
3g.46373190T>ACA352469685CCR5,CCR5ASc.288T>A (p.Phe96Leu)
n.392-1773A>T
3g.46373190T>CCA2354607CCR5,CCR5ASc.288T>C (p.Phe96=)
n.392-1773A>G
dbSNP ExAC gnomAD v2 gnomAD v4
3g.46373190T>GCA352469688CCR5,CCR5ASc.288T>G (p.Phe96Leu)
n.392-1773A>C
3g.46373190T=CA1362082479CCR5,CCR5ASc.288T= (p.Phe96=)
n.392-1773A=
3g.46373191G>ACA352469689CCR5,CCR5ASc.289G>A (p.Gly97Arg)
n.392-1774C>T
3g.46373191G>CCA352469691CCR5,CCR5ASc.289G>C (p.Gly97Arg)
n.392-1774C>G
3g.46373191G>TCA352469693CCR5,CCR5ASc.289G>T (p.Gly97Ter)
n.392-1774C>A
3g.46373191_46373192insTCTTGCTATGGGGACA2665436255CCR5,CCR5ASc.289_290insTCTTGCTATGGGGA (p.Gly97ValfsTer13)
n.392-1775_392-1774insTCCCCATAGCAAGA
gnomAD v4
3g.46373192G>ACA352469696CCR5,CCR5ASc.290G>A (p.Gly97Glu)
n.392-1775C>T
3g.46373192G>CCA352469697CCR5,CCR5ASc.290G>C (p.Gly97Ala)
n.392-1775C>G
3g.46373192G>TCA352469694CCR5,CCR5ASc.290G>T (p.Gly97Val)
n.392-1775C>A
3g.46373193A>CCA433593709CCR5,CCR5ASc.291A>C (p.Gly97=)
n.392-1776T>G
3g.46373193A>GCA433593710CCR5,CCR5ASc.291A>G (p.Gly97=)
n.392-1776T>C
COSMIC
3g.46373193A>TCA433593711CCR5,CCR5ASc.291A>T (p.Gly97=)
n.392-1776T>A
3g.46373194A>CCA352469699CCR5,CCR5ASc.292A>C (p.Asn98His)
n.392-1777T>G
3g.46373194A>GCA352469700CCR5,CCR5ASc.292A>G (p.Asn98Asp)
n.392-1777T>C
3g.46373194A>TCA352469701CCR5,CCR5ASc.292A>T (p.Asn98Tyr)
n.392-1777T>A
3g.46373195A>CCA352469704CCR5,CCR5ASc.293A>C (p.Asn98Thr)
n.392-1778T>G
3g.46373195A>GCA352469705CCR5,CCR5ASc.293A>G (p.Asn98Ser)
n.392-1778T>C
3g.46373195A>TCA352469706CCR5,CCR5ASc.293A>T (p.Asn98Ile)
n.392-1778T>A
3g.46373195_46373196insAGACACA2665436258CCR5,CCR5ASc.293_294insAGACA (p.Asn98LysfsTer9)
n.392-1778_392-1777insGTCTT
gnomAD v4
3g.46373196T>ACA352469707CCR5,CCR5ASc.294T>A (p.Asn98Lys)
n.392-1779A>T
3g.46373196T>CCA2354608CCR5,CCR5ASc.294T>C (p.Asn98=)
n.392-1779A>G
dbSNP ExAC gnomAD v2
3g.46373196T>GCA352469708CCR5,CCR5ASc.294T>G (p.Asn98Lys)
n.392-1779A>C
gnomAD v3 gnomAD v4
3g.46373196T=CA1362082480CCR5,CCR5ASc.294T= (p.Asn98=)
n.392-1779A=
3g.46373197A=CA1362082481CCR5,CCR5ASc.295A= (p.Thr99=)
n.392-1780T=
3g.46373197A>CCA352469709CCR5,CCR5ASc.295A>C (p.Thr99Pro)
n.392-1780T>G
3g.46373197A>GCA352469710CCR5,CCR5ASc.295A>G (p.Thr99Ala)
n.392-1780T>C
dbSNP gnomAD v4 COSMIC
3g.46373197A>TCA352469711CCR5,CCR5ASc.295A>T (p.Thr99Ser)
n.392-1780T>A
ClinVar
3g.46373198C>ACA352469714CCR5,CCR5ASc.296C>A (p.Thr99Lys)
n.392-1781G>T
3g.46373198C=CA1362082482CCR5,CCR5ASc.296C= (p.Thr99=)
n.392-1781G=
3g.46373198C>GCA352469712CCR5,CCR5ASc.296C>G (p.Thr99Arg)
n.392-1781G>C
3g.46373198C>TCA352469713CCR5,CCR5ASc.296C>T (p.Thr99Ile)
n.392-1781G>A
dbSNP gnomAD v2 gnomAD v4
3g.46373199A>CCA433593725CCR5,CCR5ASc.297A>C (p.Thr99=)
n.392-1782T>G
3g.46373199A>GCA433593727CCR5,CCR5ASc.297A>G (p.Thr99=)
n.392-1782T>C
3g.46373199A>TCA433593729CCR5,CCR5ASc.297A>T (p.Thr99=)
n.392-1782T>A
3g.46373200A>CCA352469715CCR5,CCR5ASc.298A>C (p.Met100Leu)
n.392-1783T>G
3g.46373200A>GCA352469716CCR5,CCR5ASc.298A>G (p.Met100Val)
n.392-1783T>C
gnomAD v4
3g.46373200A>TCA352469717CCR5,CCR5ASc.298A>T (p.Met100Leu)
n.392-1783T>A

Number of alleles fetched