Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.209625701G>ACA1375428LAMB3c.1923C>T (p.Pro641=)
c.1731C>T (p.Pro577=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.209625701G>CCA423142576LAMB3c.1923C>G (p.Pro641=)
c.1731C>G (p.Pro577=)
1g.209625701G=CA2484299205LAMB3c.1923C= (p.Pro641=)
c.1731C= (p.Pro577=)
1g.209625701G>TCA423142575LAMB3c.1923C>A (p.Pro641=)
c.1731C>A (p.Pro577=)
1g.209625704delCA2573051471LAMB3c.1923del (p.Ala642GlnfsTer?)
c.1731del (p.Ala578GlnfsTer?)
dbSNP
1g.209625702G>ACA344589126LAMB3c.1922C>T (p.Pro641Leu)
c.1730C>T (p.Pro577Leu)
COSMIC
1g.209625702G>CCA344589125LAMB3c.1922C>G (p.Pro641Arg)
c.1730C>G (p.Pro577Arg)
1g.209625702G>TCA344589127LAMB3c.1922C>A (p.Pro641His)
c.1730C>A (p.Pro577His)
1g.209625703G>ACA1375429LAMB3c.1921C>T (p.Pro641Ser)
c.1729C>T (p.Pro577Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
1g.209625703G>CCA344589128LAMB3c.1921C>G (p.Pro641Ala)
c.1729C>G (p.Pro577Ala)
1g.209625703G=CA2484299206LAMB3c.1921C= (p.Pro641=)
c.1729C= (p.Pro577=)
1g.209625703G>TCA344589129LAMB3c.1921C>A (p.Pro641Thr)
c.1729C>A (p.Pro577Thr)
dbSNP gnomAD v2 gnomAD v4
1g.209625704G>ACA423142578LAMB3c.1920C>T (p.Ser640=)
c.1728C>T (p.Ser576=)
1g.209625704G>CCA344589130LAMB3c.1920C>G (p.Ser640Arg)
c.1728C>G (p.Ser576Arg)
1g.209625704G=CA2484299207LAMB3c.1920C= (p.Ser640=)
c.1728C= (p.Ser576=)
1g.209625704G>TCA344589131LAMB3c.1920C>A (p.Ser640Arg)
c.1728C>A (p.Ser576Arg)
dbSNP gnomAD v3 gnomAD v4
1g.209625705C>ACA344589132LAMB3c.1919G>T (p.Ser640Ile)
c.1727G>T (p.Ser576Ile)
1g.209625705C=CA2484299208LAMB3c.1919G= (p.Ser640=)
c.1727G= (p.Ser576=)
1g.209625705C>GCA344589133LAMB3c.1919G>C (p.Ser640Thr)
c.1727G>C (p.Ser576Thr)
COSMIC
1g.209625705C>TCA344589134LAMB3c.1919G>A (p.Ser640Asn)
c.1727G>A (p.Ser576Asn)
dbSNP
1g.209625706T>ACA344589135LAMB3c.1918A>T (p.Ser640Cys)
c.1726A>T (p.Ser576Cys)
1g.209625706T>CCA344589136LAMB3c.1918A>G (p.Ser640Gly)
c.1726A>G (p.Ser576Gly)
dbSNP
1g.209625706T>GCA344589137LAMB3c.1918A>C (p.Ser640Arg)
c.1726A>C (p.Ser576Arg)
1g.209625706T=CA2484299209LAMB3c.1918A= (p.Ser640=)
c.1726A= (p.Ser576=)
1g.209625707G>ACA1375430LAMB3c.1917C>T (p.Ser639=)
c.1725C>T (p.Ser575=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.209625707G>CCA344589139LAMB3c.1917C>G (p.Ser639Arg)
c.1725C>G (p.Ser575Arg)
1g.209625707G=CA2484299210LAMB3c.1917C= (p.Ser639=)
c.1725C= (p.Ser575=)
1g.209625707G>TCA344589138LAMB3c.1917C>A (p.Ser639Arg)
c.1725C>A (p.Ser575Arg)
1g.209625708C>ACA344589140LAMB3c.1916G>T (p.Ser639Ile)
c.1724G>T (p.Ser575Ile)
1g.209625708C>GCA344589141LAMB3c.1916G>C (p.Ser639Thr)
c.1724G>C (p.Ser575Thr)
1g.209625708C>TCA344589142LAMB3c.1916G>A (p.Ser639Asn)
c.1724G>A (p.Ser575Asn)
1g.209625709T>ACA344589143LAMB3c.1915A>T (p.Ser639Cys)
c.1723A>T (p.Ser575Cys)
1g.209625709T>CCA344589144LAMB3c.1915A>G (p.Ser639Gly)
c.1723A>G (p.Ser575Gly)
gnomAD v4
1g.209625709T>GCA344589145LAMB3c.1915A>C (p.Ser639Arg)
c.1723A>C (p.Ser575Arg)
1g.209625710G>ACA423142579LAMB3c.1914C>T (p.Leu638=)
c.1722C>T (p.Leu574=)
1g.209625710G>CCA423142580LAMB3c.1914C>G (p.Leu638=)
c.1722C>G (p.Leu574=)
1g.209625710G>TCA423142581LAMB3c.1914C>A (p.Leu638=)
c.1722C>A (p.Leu574=)
1g.209625711A>CCA344589146LAMB3c.1913T>G (p.Leu638Arg)
c.1721T>G (p.Leu574Arg)
1g.209625711A>GCA344589147LAMB3c.1913T>C (p.Leu638Pro)
c.1721T>C (p.Leu574Pro)
1g.209625711A>TCA344589148LAMB3c.1913T>A (p.Leu638His)
c.1721T>A (p.Leu574His)
1g.209625712G>ACA344589149LAMB3c.1912C>T (p.Leu638Phe)
c.1720C>T (p.Leu574Phe)
1g.209625712G>CCA344589150LAMB3c.1912C>G (p.Leu638Val)
c.1720C>G (p.Leu574Val)
1g.209625712G>TCA344589151LAMB3c.1912C>A (p.Leu638Ile)
c.1720C>A (p.Leu574Ile)
1g.209625713A>CCA423142582LAMB3c.1911T>G (p.Val637=)
c.1719T>G (p.Val573=)
1g.209625713A>GCA423142583LAMB3c.1911T>C (p.Val637=)
c.1719T>C (p.Val573=)
1g.209625713A>TCA423142584LAMB3c.1911T>A (p.Val637=)
c.1719T>A (p.Val573=)
1g.209625714A=CA2484299211LAMB3c.1910T= (p.Val637=)
c.1718T= (p.Val573=)
1g.209625714A>CCA344589153LAMB3c.1910T>G (p.Val637Gly)
c.1718T>G (p.Val573Gly)
1g.209625714A>GCA1375431LAMB3c.1910T>C (p.Val637Ala)
c.1718T>C (p.Val573Ala)
dbSNP ExAC
1g.209625714A>TCA344589152LAMB3c.1910T>A (p.Val637Asp)
c.1718T>A (p.Val573Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4

Number of alleles fetched