Chr Mutation (hg38) CAid Gene Transcript Linkouts
1g.94060699_94062639delCA2580101943ABCA4c.1876_1999del
c.-65+536_-65+2476del (n.-65+536_-65+2476del)
ClinVar
1g.94062605_94062643delCA2580063558ABCA4c.1874_1912del (p.Gln625_Met637del)
c.-65+534_-65+572del (n.-65+534_-65+572del)
ClinVar
1g.94062615_94062620delCA2574438639ABCA4c.1894_1899del (p.Ile632_Tyr633del)
c.-65+554_-65+559del (n.-65+554_-65+559del)
1g.94062619A>CCA341279302ABCA4c.1895T>G (p.Ile632Ser)
c.-65+555T>G (n.-65+555T>G)
1g.94062619A>GCA341279304ABCA4c.1895T>C (p.Ile632Thr)
c.-65+555T>C (n.-65+555T>C)
1g.94062619A>TCA341279303ABCA4c.1895T>A (p.Ile632Asn)
c.-65+555T>A (n.-65+555T>A)
1g.94062619_94062620delinsATCA1181418813ABCA4c.1894_1895delinsAT (p.Ile632=)
c.-65+554_-65+555delinsAT (n.-65+554_-65+555delinsAT)
1g.94062620T>ACA341279305ABCA4c.1894A>T (p.Ile632Phe)
c.-65+554A>T (n.-65+554A>T)
gnomAD v4
1g.94062620T>CCA341279306ABCA4c.1894A>G (p.Ile632Val)
c.-65+554A>G (n.-65+554A>G)
1g.94062620T>GCA341279307ABCA4c.1894A>C (p.Ile632Leu)
c.-65+554A>C (n.-65+554A>C)
1g.94062620_94062621delinsTTCA1140726066ABCA4c.1893_1894delinsAA (p.Gly631=)
c.-65+553_-65+554delinsAA (n.-65+553_-65+554delinsAA)
1g.94062621delCA226947ABCA4c.1894del (p.Ile632SerfsTer17)
c.-65+554del (n.-65+554del)
ClinVar dbSNP
1g.94062621T>ACA418822042ABCA4c.1893A>T (p.Gly631=)
c.-65+553A>T (n.-65+553A>T)
1g.94062621T>CCA418822043ABCA4c.1893A>G (p.Gly631=)
c.-65+553A>G (n.-65+553A>G)
1g.94062621T>GCA418822044ABCA4c.1893A>C (p.Gly631=)
c.-65+553A>C (n.-65+553A>C)
1g.94062622C>ACA341279310ABCA4c.1892G>T (p.Gly631Val)
c.-65+552G>T (n.-65+552G>T)
ClinVar dbSNP gnomAD v2
1g.94062622C=CA1181418814ABCA4c.1892G= (p.Gly631=)
c.-65+552G= (n.-65+552G=)
1g.94062622C>GCA341279308ABCA4c.1892G>C (p.Gly631Ala)
c.-65+552G>C (n.-65+552G>C)
1g.94062622C>TCA341279309ABCA4c.1892G>A (p.Gly631Glu)
c.-65+552G>A (n.-65+552G>A)
ClinVar gnomAD v4
1g.94062623C>ACA341279311ABCA4c.1891G>T (p.Gly631Ter)
c.-65+551G>T (n.-65+551G>T)
1g.94062623C=CA1181418815ABCA4c.1891G= (p.Gly631=)
c.-65+551G= (n.-65+551G=)
1g.94062623C>GCA341279312ABCA4c.1891G>C (p.Gly631Arg)
c.-65+551G>C (n.-65+551G>C)
1g.94062623C>TCA10602445ABCA4c.1891G>A (p.Gly631Arg)
c.-65+551G>A (n.-65+551G>A)
ClinVar dbSNP
1g.94062624A>CCA418822046ABCA4c.1890T>G (p.Val630=)
c.-65+550T>G (n.-65+550T>G)
1g.94062624A>GCA418822048ABCA4c.1890T>C (p.Val630=)
c.-65+550T>C (n.-65+550T>C)
1g.94062624A>TCA418822050ABCA4c.1890T>A (p.Val630=)
c.-65+550T>A (n.-65+550T>A)
1g.94062625A>CCA341279313ABCA4c.1889T>G (p.Val630Gly)
c.-65+549T>G (n.-65+549T>G)
1g.94062625A>GCA341279314ABCA4c.1889T>C (p.Val630Ala)
c.-65+549T>C (n.-65+549T>C)
1g.94062625A>TCA341279315ABCA4c.1889T>A (p.Val630Asp)
c.-65+549T>A (n.-65+549T>A)
gnomAD v4
1g.94062626delCA2739272683ABCA4c.1888del (p.Val630LeufsTer19)
c.-65+548del (n.-65+548del)
ClinVar
1g.94062626C>ACA341279316ABCA4c.1888G>T (p.Val630Phe)
c.-65+548G>T (n.-65+548G>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
1g.94062626C=CA1181418816ABCA4c.1888G= (p.Val630=)
c.-65+548G= (n.-65+548G=)
1g.94062626C>GCA341279317ABCA4c.1888G>C (p.Val630Leu)
c.-65+548G>C (n.-65+548G>C)
1g.94062626C>TCA341279318ABCA4c.1888G>A (p.Val630Ile)
c.-65+548G>A (n.-65+548G>A)
1g.94062627T>ACA418822052ABCA4c.1887A>T (p.Pro629=)
c.-65+547A>T (n.-65+547A>T)
gnomAD v4
1g.94062627T>CCA418822053ABCA4c.1887A>G (p.Pro629=)
c.-65+547A>G (n.-65+547A>G)
gnomAD v4
1g.94062627T>GCA418822054ABCA4c.1887A>C (p.Pro629=)
c.-65+547A>C (n.-65+547A>C)
dbSNP gnomAD v2 gnomAD v4
1g.94062627T=CA1181418817ABCA4c.1887A= (p.Pro629=)
c.-65+547A= (n.-65+547A=)
1g.94062628G>ACA958403ABCA4c.1886C>T (p.Pro629Leu)
c.-65+546C>T (n.-65+546C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
1g.94062628G>CCA341279319ABCA4c.1886C>G (p.Pro629Arg)
c.-65+546C>G (n.-65+546C>G)
1g.94062628G=CA1181418818ABCA4c.1886C= (p.Pro629=)
c.-65+546C= (n.-65+546C=)
1g.94062628G>TCA341279320ABCA4c.1886C>A (p.Pro629Gln)
c.-65+546C>A (n.-65+546C>A)
1g.94062629G>ACA341279321ABCA4c.1885C>T (p.Pro629Ser)
c.-65+545C>T (n.-65+545C>T)
1g.94062629G>CCA341279323ABCA4c.1885C>G (p.Pro629Ala)
c.-65+545C>G (n.-65+545C>G)
ClinVar dbSNP gnomAD v3 gnomAD v4
1g.94062629G=CA1181418819ABCA4c.1885C= (p.Pro629=)
c.-65+545C= (n.-65+545C=)
1g.94062629G>TCA341279322ABCA4c.1885C>A (p.Pro629Thr)
c.-65+545C>A (n.-65+545C>A)
1g.94062630A>CCA418822058ABCA4c.1884T>G (p.Ala628=)
c.-65+544T>G (n.-65+544T>G)
1g.94062630A>GCA418822059ABCA4c.1884T>C (p.Ala628=)
c.-65+544T>C (n.-65+544T>C)
1g.94062630A>TCA418822060ABCA4c.1884T>A (p.Ala628=)
c.-65+544T>A (n.-65+544T>A)
COSMIC COSMIC
1g.94062631G>ACA26848044ABCA4c.1883C>T (p.Ala628Val)
c.-65+543C>T (n.-65+543C>T)
dbSNP gnomAD v4

Number of alleles fetched