Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.2277929T>ACA394304431ABCA3c.4859A>T (p.Gln1620Leu)
c.4685A>T (p.Gln1562Leu)
16g.2277929T>CCA394304437ABCA3c.4859A>G (p.Gln1620Arg)
c.4685A>G (p.Gln1562Arg)
16g.2277929T>GCA394304434ABCA3c.4859A>C (p.Gln1620Pro)
c.4685A>C (p.Gln1562Pro)
16g.2277930G>ACA394304443ABCA3c.4858C>T (p.Gln1620Ter)
c.4684C>T (p.Gln1562Ter)
ClinVar
16g.2277930G>CCA394304446ABCA3c.4858C>G (p.Gln1620Glu)
c.4684C>G (p.Gln1562Glu)
16g.2277930G>TCA394304448ABCA3c.4858C>A (p.Gln1620Lys)
c.4684C>A (p.Gln1562Lys)
16g.2277931C>ACA493360588ABCA3c.4857G>T (p.Gly1619=)
c.4683G>T (p.Gly1561=)
16g.2277931C=CA2202146047ABCA3c.4857G= (p.Gly1619=)
c.4683G= (p.Gly1561=)
16g.2277931C>GCA493360589ABCA3c.4857G>C (p.Gly1619=)
c.4683G>C (p.Gly1561=)
16g.2277931C>TCA7840002ABCA3c.4857G>A (p.Gly1619=)
c.4683G>A (p.Gly1561=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.2277932C>ACA394304455ABCA3c.4856G>T (p.Gly1619Val)
c.4682G>T (p.Gly1561Val)
gnomAD v4
16g.2277932C>GCA394304459ABCA3c.4856G>C (p.Gly1619Ala)
c.4682G>C (p.Gly1561Ala)
16g.2277932C>TCA394304462ABCA3c.4856G>A (p.Gly1619Glu)
c.4682G>A (p.Gly1561Glu)
16g.2277936_2277948delCA2695221869ABCA3c.4844_4856del (p.Val1615GlyfsTer15)
c.4670_4682del (p.Val1557GlyfsTer15)
16g.2277933C>ACA394304476ABCA3c.4855G>T (p.Gly1619Trp)
c.4681G>T (p.Gly1561Trp)
16g.2277933C=CA2202146048ABCA3c.4855G= (p.Gly1619=)
c.4681G= (p.Gly1561=)
16g.2277933C>GCA394304478ABCA3c.4855G>C (p.Gly1619Arg)
c.4681G>C (p.Gly1561Arg)
gnomAD v4
16g.2277933C>TCA394304480ABCA3c.4855G>A (p.Gly1619Arg)
c.4681G>A (p.Gly1561Arg)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
16g.2277934T>ACA394304482ABCA3c.4854A>T (p.Glu1618Asp)
c.4680A>T (p.Glu1560Asp)
16g.2277934T>CCA493360590ABCA3c.4854A>G (p.Glu1618=)
c.4680A>G (p.Glu1560=)
16g.2277934T>GCA394304483ABCA3c.4854A>C (p.Glu1618Asp)
c.4680A>C (p.Glu1560Asp)
gnomAD v4
16g.2277935T>ACA394304491ABCA3c.4853A>T (p.Glu1618Val)
c.4679A>T (p.Glu1560Val)
16g.2277935T>CCA7840003ABCA3c.4853A>G (p.Glu1618Gly)
c.4679A>G (p.Glu1560Gly)
dbSNP ExAC gnomAD v2 gnomAD v4
16g.2277935T>GCA394304488ABCA3c.4853A>C (p.Glu1618Ala)
c.4679A>C (p.Glu1560Ala)
16g.2277935T=CA2202146049ABCA3c.4853A= (p.Glu1618=)
c.4679A= (p.Glu1560=)
16g.2277936C>ACA394304495ABCA3c.4852G>T (p.Glu1618Ter)
c.4678G>T (p.Glu1560Ter)
16g.2277936C>GCA394304498ABCA3c.4852G>C (p.Glu1618Gln)
c.4678G>C (p.Glu1560Gln)
16g.2277936C>TCA394304499ABCA3c.4852G>A (p.Glu1618Lys)
c.4678G>A (p.Glu1560Lys)
gnomAD v4
16g.2277937A=CA2202146050ABCA3c.4851T= (p.Ser1617=)
c.4677T= (p.Ser1559=)
16g.2277937A>CCA394304504ABCA3c.4851T>G (p.Ser1617Arg)
c.4677T>G (p.Ser1559Arg)
dbSNP gnomAD v3 gnomAD v4
16g.2277937A>GCA493360591ABCA3c.4851T>C (p.Ser1617=)
c.4677T>C (p.Ser1559=)
16g.2277937A>TCA394304506ABCA3c.4851T>A (p.Ser1617Arg)
c.4677T>A (p.Ser1559Arg)
16g.2277938C>ACA394304510ABCA3c.4850G>T (p.Ser1617Ile)
c.4676G>T (p.Ser1559Ile)
16g.2277938C=CA2202146051ABCA3c.4850G= (p.Ser1617=)
c.4676G= (p.Ser1559=)
16g.2277938C>GCA394304512ABCA3c.4850G>C (p.Ser1617Thr)
c.4676G>C (p.Ser1559Thr)
dbSNP gnomAD v3 gnomAD v4
16g.2277938C>TCA394304514ABCA3c.4850G>A (p.Ser1617Asn)
c.4676G>A (p.Ser1559Asn)
gnomAD v4
16g.2277939T>ACA394304518ABCA3c.4849A>T (p.Ser1617Cys)
c.4675A>T (p.Ser1559Cys)
16g.2277939T>CCA394304519ABCA3c.4849A>G (p.Ser1617Gly)
c.4675A>G (p.Ser1559Gly)
16g.2277939T>GCA394304520ABCA3c.4849A>C (p.Ser1617Arg)
c.4675A>C (p.Ser1559Arg)
dbSNP gnomAD v3 gnomAD v4
16g.2277939T=CA2202146052ABCA3c.4849A= (p.Ser1617=)
c.4675A= (p.Ser1559=)
16g.2277940C>ACA394304524ABCA3c.4848G>T (p.Gln1616His)
c.4674G>T (p.Gln1558His)
16g.2277940C>GCA394304522ABCA3c.4848G>C (p.Gln1616His)
c.4674G>C (p.Gln1558His)
16g.2277940C>TCA493360592ABCA3c.4848G>A (p.Gln1616=)
c.4674G>A (p.Gln1558=)
16g.2277941T>ACA394304528ABCA3c.4847A>T (p.Gln1616Leu)
c.4673A>T (p.Gln1558Leu)
16g.2277941T>CCA394304529ABCA3c.4847A>G (p.Gln1616Arg)
c.4673A>G (p.Gln1558Arg)
gnomAD v4
16g.2277941T>GCA394304531ABCA3c.4847A>C (p.Gln1616Pro)
c.4673A>C (p.Gln1558Pro)
16g.2277942G>ACA394304534ABCA3c.4846C>T (p.Gln1616Ter)
c.4672C>T (p.Gln1558Ter)
16g.2277942G>CCA394304537ABCA3c.4846C>G (p.Gln1616Glu)
c.4672C>G (p.Gln1558Glu)
16g.2277942G>TCA394304542ABCA3c.4846C>A (p.Gln1616Lys)
c.4672C>A (p.Gln1558Lys)
16g.2277943C>ACA493360593ABCA3c.4845G>T (p.Val1615=)
c.4671G>T (p.Val1557=)

Number of alleles fetched