Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.120739122C=CA2067555696ACADSc.1030-18C= (n.1030-18C=)
c.1018-18C= (n.1018-18C=)
12g.120739122C>TCA952544134ACADSc.1030-18C>T (n.1030-18C>T)
c.1018-18C>T (n.1018-18C>T)
dbSNP gnomAD v3 gnomAD v4
12g.120739123T>CCA608059970ACADSc.1030-17T>C (n.1030-17T>C)
c.1018-17T>C (n.1018-17T>C)
dbSNP gnomAD v2 gnomAD v4
12g.120739123T=CA2067555697ACADSc.1030-17T= (n.1030-17T=)
c.1018-17T= (n.1018-17T=)
12g.120739124_120739125delCA2621370030ACADSc.1030-16_1030-15del (n.1030-16_1030-15del)
c.1018-16_1018-15del (n.1018-16_1018-15del)
gnomAD v4
12g.120739124G>ACA2575321542ACADSc.1030-16G>A (n.1030-16G>A)
c.1018-16G>A (n.1018-16G>A)
gnomAD v4
12g.120739126A=CA2067555698ACADSc.1030-14A= (n.1030-14A=)
c.1018-14A= (n.1018-14A=)
12g.120739126A>CCA2067555699ACADSc.1030-14A>C (n.1030-14A>C)
c.1018-14A>C (n.1018-14A>C)
dbSNP
12g.120739127C>ACA2621370037ACADSc.1030-13C>A (n.1030-13C>A)
c.1018-13C>A (n.1018-13C>A)
gnomAD v4
12g.120739127C=CA2067555700ACADSc.1030-13C= (n.1030-13C=)
c.1018-13C= (n.1018-13C=)
12g.120739127C>TCA6831190ACADSc.1030-13C>T (n.1030-13C>T)
c.1018-13C>T (n.1018-13C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.120739131delCA2621370034ACADSc.1030-9del (n.1030-9del)
c.1018-9del (n.1018-9del)
gnomAD v4
12g.120739128C=CA2067555701ACADSc.1030-12C= (n.1030-12C=)
c.1018-12C= (n.1018-12C=)
12g.120739128C>TCA2067555702ACADSc.1030-12C>T (n.1030-12C>T)
c.1018-12C>T (n.1018-12C>T)
dbSNP
12g.120739129C=CA2067555703ACADSc.1030-11C= (n.1030-11C=)
c.1018-11C= (n.1018-11C=)
12g.120739129C>GCA608059971ACADSc.1030-11C>G (n.1030-11C>G)
c.1018-11C>G (n.1018-11C>G)
dbSNP gnomAD v2 gnomAD v4
12g.120739129C>TCA6831191ACADSc.1030-11C>T (n.1030-11C>T)
c.1018-11C>T (n.1018-11C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739130C>TCA2621370047ACADSc.1030-10C>T (n.1030-10C>T)
c.1018-10C>T (n.1018-10C>T)
gnomAD v4
12g.120739131C=CA2067555704ACADSc.1030-9C= (n.1030-9C=)
c.1018-9C= (n.1018-9C=)
12g.120739131C>TCA913786492ACADSc.1030-9C>T (n.1030-9C>T)
c.1018-9C>T (n.1018-9C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739132A=CA2067555705ACADSc.1030-8A= (n.1030-8A=)
c.1018-8A= (n.1018-8A=)
12g.120739132A>TCA2067555706ACADSc.1030-8A>T (n.1030-8A>T)
c.1018-8A>T (n.1018-8A>T)
dbSNP
12g.120739132dupCA244495137ACADSc.1030-8dup (n.1030-8dup)
c.1018-8dup (n.1018-8dup)
dbSNP
12g.120739133T>ACA2621370055ACADSc.1030-7T>A (n.1030-7T>A)
c.1018-7T>A (n.1018-7T>A)
gnomAD v4
12g.120739133T>CCA952544140ACADSc.1030-7T>C (n.1030-7T>C)
c.1018-7T>C (n.1018-7T>C)
dbSNP gnomAD v3 gnomAD v4
12g.120739133T>GCA2621370054ACADSc.1030-7T>G (n.1030-7T>G)
c.1018-7T>G (n.1018-7T>G)
gnomAD v4
12g.120739133T=CA2067555707ACADSc.1030-7T= (n.1030-7T=)
c.1018-7T= (n.1018-7T=)
12g.120739134G>ACA482146803ACADSc.1030-6G>A (n.1030-6G>A)
c.1018-6G>A (n.1018-6G>A)
ClinVar dbSNP gnomAD v4
12g.120739134G=CA2067555708ACADSc.1030-6G= (n.1030-6G=)
c.1018-6G= (n.1018-6G=)
12g.120739136T>GCA2067555710ACADSc.1030-4T>G (n.1030-4T>G)
c.1018-4T>G (n.1018-4T>G)
dbSNP gnomAD v4
12g.120739136T=CA2067555709ACADSc.1030-4T= (n.1030-4T=)
c.1018-4T= (n.1018-4T=)
12g.120739137_120739154dupCA1139662939ACADSc.1030-3_1044dup
c.1018-3_1032dup
ClinVar dbSNP
12g.120739138A>CCA386601622ACADSc.1030-2A>C (n.1030-2A>C)
c.1018-2A>C (n.1018-2A>C)
12g.120739138A>GCA386601623ACADSc.1030-2A>G (n.1030-2A>G)
c.1018-2A>G (n.1018-2A>G)
12g.120739138A>TCA386601624ACADSc.1030-2A>T (n.1030-2A>T)
c.1018-2A>T (n.1018-2A>T)
12g.120739139G>ACA386601625ACADSc.1030-1G>A (n.1030-1G>A)
c.1018-1G>A (n.1018-1G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.120739139G>CCA386601626ACADSc.1030-1G>C (n.1030-1G>C)
c.1018-1G>C (n.1018-1G>C)
12g.120739139G=CA2067555711ACADSc.1030-1G= (n.1030-1G=)
c.1018-1G= (n.1018-1G=)
12g.120739139G>TCA386601627ACADSc.1030-1G>T (n.1030-1G>T)
c.1018-1G>T (n.1018-1G>T)
12g.120739140G>ACA386601628ACADSc.1030G>A (p.Glu344Lys)
c.1018G>A (p.Glu340Lys)
dbSNP
12g.120739140G>CCA386601629ACADSc.1030G>C (p.Glu344Gln)
c.1018G>C (p.Glu340Gln)
12g.120739140G=CA2067555713ACADSc.1030G= (p.Glu344=)
c.1018G= (p.Glu340=)
12g.120739140G>TCA386601630ACADSc.1030G>T (p.Glu344Ter)
c.1018G>T (p.Glu340Ter)
12g.120739140_120739141delinsGACA2067555712ACADSc.1030_1031delinsGA (p.Glu344=)
c.1018_1019delinsGA (p.Glu340=)
12g.120739141delCA16041573ACADSc.1031del (p.Glu344GlyfsTer30)
c.1019del (p.Glu340GlyfsTer30)
ClinVar dbSNP
12g.120739141A=CA2067555714ACADSc.1031A= (p.Glu344=)
c.1019A= (p.Glu340=)
12g.120739141A>CCA386601631ACADSc.1031A>C (p.Glu344Ala)
c.1019A>C (p.Glu340Ala)
12g.120739141A>GCA259859ACADSc.1031A>G (p.Glu344Gly)
c.1019A>G (p.Glu340Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.120739141A>TCA386601632ACADSc.1031A>T (p.Glu344Val)
c.1019A>T (p.Glu340Val)
12g.120739142G>ACA482146811ACADSc.1032G>A (p.Glu344=)
c.1020G>A (p.Glu340=)
12g.120739142G>CCA386601633ACADSc.1032G>C (p.Glu344Asp)
c.1020G>C (p.Glu340Asp)
gnomAD v4
12g.120739142G>TCA386601634ACADSc.1032G>T (p.Glu344Asp)
c.1020G>T (p.Glu340Asp)
12g.120739143G>ACA386601635ACADSc.1033G>A (p.Ala345Thr)
c.1021G>A (p.Ala341Thr)
12g.120739143G>CCA386601636ACADSc.1033G>C (p.Ala345Pro)
c.1021G>C (p.Ala341Pro)
12g.120739143G=CA2067555715ACADSc.1033G= (p.Ala345=)
c.1021G= (p.Ala341=)
12g.120739143G>TCA6831192ACADSc.1033G>T (p.Ala345Ser)
c.1021G>T (p.Ala341Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739144C>ACA386601637ACADSc.1034C>A (p.Ala345Glu)
c.1022C>A (p.Ala341Glu)
12g.120739144C=CA2067555716ACADSc.1034C= (p.Ala345=)
c.1022C= (p.Ala341=)
12g.120739144C>GCA386601638ACADSc.1034C>G (p.Ala345Gly)
c.1022C>G (p.Ala341Gly)
12g.120739144C>TCA386601639ACADSc.1034C>T (p.Ala345Val)
c.1022C>T (p.Ala341Val)
dbSNP
12g.120739145A>CCA482146814ACADSc.1035A>C (p.Ala345=)
c.1023A>C (p.Ala341=)
12g.120739145A>GCA482146815ACADSc.1035A>G (p.Ala345=)
c.1023A>G (p.Ala341=)
12g.120739145A>TCA482146816ACADSc.1035A>T (p.Ala345=)
c.1023A>T (p.Ala341=)
12g.120739146G>ACA386601640ACADSc.1036G>A (p.Ala346Thr)
c.1024G>A (p.Ala342Thr)
12g.120739146G>CCA386601641ACADSc.1036G>C (p.Ala346Pro)
c.1024G>C (p.Ala342Pro)
12g.120739146G>TCA386601642ACADSc.1036G>T (p.Ala346Ser)
c.1024G>T (p.Ala342Ser)
12g.120739147C>ACA386601645ACADSc.1037C>A (p.Ala346Asp)
c.1025C>A (p.Ala342Asp)
12g.120739147C>GCA386601644ACADSc.1037C>G (p.Ala346Gly)
c.1025C>G (p.Ala342Gly)
12g.120739147C>TCA386601643ACADSc.1037C>T (p.Ala346Val)
c.1025C>T (p.Ala342Val)
12g.120739148C>ACA482146821ACADSc.1038C>A (p.Ala346=)
c.1026C>A (p.Ala342=)
12g.120739148C>GCA482146823ACADSc.1038C>G (p.Ala346=)
c.1026C>G (p.Ala342=)
12g.120739148C>TCA482146822ACADSc.1038C>T (p.Ala346=)
c.1026C>T (p.Ala342=)
12g.120739149A=CA2067555717ACADSc.1039A= (p.Met347=)
c.1027A= (p.Met343=)
12g.120739149A>CCA386601646ACADSc.1039A>C (p.Met347Leu)
c.1027A>C (p.Met343Leu)
12g.120739149A>GCA312224ACADSc.1039A>G (p.Met347Val)
c.1027A>G (p.Met343Val)
dbSNP
12g.120739149A>TCA386601647ACADSc.1039A>T (p.Met347Leu)
c.1027A>T (p.Met343Leu)
12g.120739150T>ACA386601648ACADSc.1040T>A (p.Met347Lys)
c.1028T>A (p.Met343Lys)
12g.120739150T>CCA386601649ACADSc.1040T>C (p.Met347Thr)
c.1028T>C (p.Met343Thr)
12g.120739150T>GCA386601650ACADSc.1040T>G (p.Met347Arg)
c.1028T>G (p.Met343Arg)
12g.120739150T=CA2067555718ACADSc.1040T= (p.Met347=)
c.1028T= (p.Met343=)
12g.120739151G>ACA386601651ACADSc.1041G>A (p.Met347Ile)
c.1029G>A (p.Met343Ile)
12g.120739151G>CCA386601652ACADSc.1041G>C (p.Met347Ile)
c.1029G>C (p.Met343Ile)
12g.120739151G>TCA386601653ACADSc.1041G>T (p.Met347Ile)
c.1029G>T (p.Met343Ile)
12g.120739152dupCA684418892ACADSc.1042dup (p.Ala348GlyfsTer?)
c.1030dup (p.Ala344GlyfsTer?)
dbSNP gnomAD v3 gnomAD v4
12g.120739152G>ACA386601654ACADSc.1042G>A (p.Ala348Thr)
c.1030G>A (p.Ala344Thr)
12g.120739152G>CCA386601655ACADSc.1042G>C (p.Ala348Pro)
c.1030G>C (p.Ala344Pro)
12g.120739152G>TCA386601656ACADSc.1042G>T (p.Ala348Ser)
c.1030G>T (p.Ala344Ser)
gnomAD v4
12g.120739153C>ACA386601659ACADSc.1043C>A (p.Ala348Asp)
c.1031C>A (p.Ala344Asp)
12g.120739153C>GCA386601658ACADSc.1043C>G (p.Ala348Gly)
c.1031C>G (p.Ala344Gly)
12g.120739153C>TCA386601657ACADSc.1043C>T (p.Ala348Val)
c.1031C>T (p.Ala344Val)
12g.120739154C>ACA482146831ACADSc.1044C>A (p.Ala348=)
c.1032C>A (p.Ala344=)
12g.120739154C>GCA482146835ACADSc.1044C>G (p.Ala348=)
c.1032C>G (p.Ala344=)
12g.120739154C>TCA482146833ACADSc.1044C>T (p.Ala348=)
c.1032C>T (p.Ala344=)
12g.120739155A>CCA386601660ACADSc.1045A>C (p.Lys349Gln)
c.1033A>C (p.Lys345Gln)
12g.120739155A>GCA386601662ACADSc.1045A>G (p.Lys349Glu)
c.1033A>G (p.Lys345Glu)
12g.120739155A>TCA386601661ACADSc.1045A>T (p.Lys349Ter)
c.1033A>T (p.Lys345Ter)
12g.120739156A>CCA386601663ACADSc.1046A>C (p.Lys349Thr)
c.1034A>C (p.Lys345Thr)
12g.120739156A>GCA386601665ACADSc.1046A>G (p.Lys349Arg)
c.1034A>G (p.Lys345Arg)
12g.120739156A>TCA386601664ACADSc.1046A>T (p.Lys349Met)
c.1034A>T (p.Lys345Met)
12g.120739157G>ACA482146839ACADSc.1047G>A (p.Lys349=)
c.1035G>A (p.Lys345=)
12g.120739157G>CCA386601666ACADSc.1047G>C (p.Lys349Asn)
c.1035G>C (p.Lys345Asn)
12g.120739157G>TCA386601667ACADSc.1047G>T (p.Lys349Asn)
c.1035G>T (p.Lys345Asn)
12g.120739158C>ACA386601668ACADSc.1048C>A (p.Leu350Met)
c.1036C>A (p.Leu346Met)
12g.120739158C>GCA386601669ACADSc.1048C>G (p.Leu350Val)
c.1036C>G (p.Leu346Val)
12g.120739158C>TCA482146841ACADSc.1048C>T (p.Leu350=)
c.1036C>T (p.Leu346=)
gnomAD v4
12g.120739159T>ACA386601670ACADSc.1049T>A (p.Leu350Gln)
c.1037T>A (p.Leu346Gln)
12g.120739159T>CCA386601671ACADSc.1049T>C (p.Leu350Pro)
c.1037T>C (p.Leu346Pro)
12g.120739159T>GCA386601672ACADSc.1049T>G (p.Leu350Arg)
c.1037T>G (p.Leu346Arg)
12g.120739160G>ACA482146845ACADSc.1050G>A (p.Leu350=)
c.1038G>A (p.Leu346=)
gnomAD v4
12g.120739160G>CCA482146846ACADSc.1050G>C (p.Leu350=)
c.1038G>C (p.Leu346=)
12g.120739160G=CA2067555719ACADSc.1050G= (p.Leu350=)
c.1038G= (p.Leu346=)
12g.120739160G>TCA6831193ACADSc.1050G>T (p.Leu350=)
c.1038G>T (p.Leu346=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739161G>ACA386601673ACADSc.1051G>A (p.Ala351Thr)
c.1039G>A (p.Ala347Thr)
dbSNP gnomAD v2
12g.120739161G>CCA386601674ACADSc.1051G>C (p.Ala351Pro)
c.1039G>C (p.Ala347Pro)
12g.120739161G=CA2067555720ACADSc.1051G= (p.Ala351=)
c.1039G= (p.Ala347=)
12g.120739161G>TCA386601675ACADSc.1051G>T (p.Ala351Ser)
c.1039G>T (p.Ala347Ser)
dbSNP
12g.120739162C>ACA386601677ACADSc.1052C>A (p.Ala351Asp)
c.1040C>A (p.Ala347Asp)
dbSNP
12g.120739162C=CA2067555721ACADSc.1052C= (p.Ala351=)
c.1040C= (p.Ala347=)
12g.120739162C>GCA386601676ACADSc.1052C>G (p.Ala351Gly)
c.1040C>G (p.Ala347Gly)
12g.120739162C>TCA6831194ACADSc.1052C>T (p.Ala351Val)
c.1040C>T (p.Ala347Val)
dbSNP ExAC gnomAD v2
12g.120739163C>ACA482146849ACADSc.1053C>A (p.Ala351=)
c.1041C>A (p.Ala347=)
gnomAD v4
12g.120739163C=CA2067555722ACADSc.1053C= (p.Ala351=)
c.1041C= (p.Ala347=)
12g.120739163C>GCA482146848ACADSc.1053C>G (p.Ala351=)
c.1041C>G (p.Ala347=)
12g.120739163C>TCA6831195ACADSc.1053C>T (p.Ala351=)
c.1041C>T (p.Ala347=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739164G>ACA6831196ACADSc.1054G>A (p.Ala352Thr)
c.1042G>A (p.Ala348Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739164G>CCA386601678ACADSc.1054G>C (p.Ala352Pro)
c.1042G>C (p.Ala348Pro)
12g.120739164G=CA2067555723ACADSc.1054G= (p.Ala352=)
c.1042G= (p.Ala348=)
12g.120739164G>TCA6831197ACADSc.1054G>T (p.Ala352Ser)
c.1042G>T (p.Ala348Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739165C>ACA386601679ACADSc.1055C>A (p.Ala352Asp)
c.1043C>A (p.Ala348Asp)
12g.120739165C>GCA386601680ACADSc.1055C>G (p.Ala352Gly)
c.1043C>G (p.Ala348Gly)
12g.120739165C>TCA386601681ACADSc.1055C>T (p.Ala352Val)
c.1043C>T (p.Ala348Val)
12g.120739166C>ACA482146851ACADSc.1056C>A (p.Ala352=)
c.1044C>A (p.Ala348=)
12g.120739166C>GCA482146852ACADSc.1056C>G (p.Ala352=)
c.1044C>G (p.Ala348=)
12g.120739166C>TCA482146853ACADSc.1056C>T (p.Ala352=)
c.1044C>T (p.Ala348=)
12g.120739167T>ACA386601682ACADSc.1057T>A (p.Ser353Thr)
c.1045T>A (p.Ser349Thr)
12g.120739167T>CCA312226ACADSc.1057T>C (p.Ser353Pro)
c.1045T>C (p.Ser349Pro)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739167T>GCA386601683ACADSc.1057T>G (p.Ser353Ala)
c.1045T>G (p.Ser349Ala)
12g.120739167T=CA2067555724ACADSc.1057T= (p.Ser353=)
c.1045T= (p.Ser349=)
12g.120739168C>ACA386601684ACADSc.1058C>A (p.Ser353Ter)
c.1046C>A (p.Ser349Ter)
12g.120739168C=CA2067555725ACADSc.1058C= (p.Ser353=)
c.1046C= (p.Ser349=)
12g.120739168C>GCA386601685ACADSc.1058C>G (p.Ser353Trp)
c.1046C>G (p.Ser349Trp)
12g.120739168C>TCA252888ACADSc.1058C>T (p.Ser353Leu)
c.1046C>T (p.Ser349Leu)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739169G>ACA482146855ACADSc.1059G>A (p.Ser353=)
c.1047G>A (p.Ser349=)
dbSNP gnomAD v3 gnomAD v4
12g.120739169G>CCA482146856ACADSc.1059G>C (p.Ser353=)
c.1047G>C (p.Ser349=)
12g.120739169G=CA2067555726ACADSc.1059G= (p.Ser353=)
c.1047G= (p.Ser349=)
12g.120739169G>TCA482146857ACADSc.1059G>T (p.Ser353=)
c.1047G>T (p.Ser349=)
12g.120739170G>ACA244495188ACADSc.1060G>A (p.Glu354Lys)
c.1048G>A (p.Glu350Lys)
dbSNP
12g.120739170G>CCA386601686ACADSc.1060G>C (p.Glu354Gln)
c.1048G>C (p.Glu350Gln)
12g.120739170G=CA2067555727ACADSc.1060G= (p.Glu354=)
c.1048G= (p.Glu350=)
12g.120739170G>TCA386601687ACADSc.1060G>T (p.Glu354Ter)
c.1048G>T (p.Glu350Ter)
12g.120739171A>CCA386601688ACADSc.1061A>C (p.Glu354Ala)
c.1049A>C (p.Glu350Ala)
12g.120739171A>GCA386601689ACADSc.1061A>G (p.Glu354Gly)
c.1049A>G (p.Glu350Gly)
12g.120739171A>TCA386601690ACADSc.1061A>T (p.Glu354Val)
c.1049A>T (p.Glu350Val)
12g.120739172G>ACA482146858ACADSc.1062G>A (p.Glu354=)
c.1050G>A (p.Glu350=)
12g.120739172G>CCA386601691ACADSc.1062G>C (p.Glu354Asp)
c.1050G>C (p.Glu350Asp)
12g.120739172G>TCA386601692ACADSc.1062G>T (p.Glu354Asp)
c.1050G>T (p.Glu350Asp)
12g.120739173G>ACA386601693ACADSc.1063G>A (p.Ala355Thr)
c.1051G>A (p.Ala351Thr)
12g.120739173G>CCA386601694ACADSc.1063G>C (p.Ala355Pro)
c.1051G>C (p.Ala351Pro)
12g.120739173G>TCA386601695ACADSc.1063G>T (p.Ala355Ser)
c.1051G>T (p.Ala351Ser)
12g.120739174C>ACA386601696ACADSc.1064C>A (p.Ala355Asp)
c.1052C>A (p.Ala351Asp)
12g.120739174C=CA2067555728ACADSc.1064C= (p.Ala355=)
c.1052C= (p.Ala351=)
12g.120739174C>GCA386601697ACADSc.1064C>G (p.Ala355Gly)
c.1052C>G (p.Ala351Gly)
12g.120739174C>TCA6831198ACADSc.1064C>T (p.Ala355Val)
c.1052C>T (p.Ala351Val)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
12g.120739175C>ACA482146862ACADSc.1065C>A (p.Ala355=)
c.1053C>A (p.Ala351=)
12g.120739175C=CA2067555729ACADSc.1065C= (p.Ala355=)
c.1053C= (p.Ala351=)
12g.120739175C>GCA244495193ACADSc.1065C>G (p.Ala355=)
c.1053C>G (p.Ala351=)
dbSNP
12g.120739175C>TCA6831199ACADSc.1065C>T (p.Ala355=)
c.1053C>T (p.Ala351=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739176G>ACA244495195ACADSc.1066G>A (p.Ala356Thr)
c.1054G>A (p.Ala352Thr)
ClinVar dbSNP gnomAD v4
12g.120739176G>CCA386601698ACADSc.1066G>C (p.Ala356Pro)
c.1054G>C (p.Ala352Pro)
12g.120739176G=CA2067555730ACADSc.1066G= (p.Ala356=)
c.1054G= (p.Ala352=)
12g.120739176G>TCA386601699ACADSc.1066G>T (p.Ala356Ser)
c.1054G>T (p.Ala352Ser)
dbSNP
12g.120739177C>ACA386601700ACADSc.1067C>A (p.Ala356Glu)
c.1055C>A (p.Ala352Glu)
12g.120739177C=CA2067555731ACADSc.1067C= (p.Ala356=)
c.1055C= (p.Ala352=)
12g.120739177C>GCA386601701ACADSc.1067C>G (p.Ala356Gly)
c.1055C>G (p.Ala352Gly)
12g.120739177C>TCA386601702ACADSc.1067C>T (p.Ala356Val)
c.1055C>T (p.Ala352Val)
ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC
12g.120739178G>ACA244495200ACADSc.1068G>A (p.Ala356=)
c.1056G>A (p.Ala352=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739178G>CCA482146864ACADSc.1068G>C (p.Ala356=)
c.1056G>C (p.Ala352=)
12g.120739178G=CA2067555732ACADSc.1068G= (p.Ala356=)
c.1056G= (p.Ala352=)
12g.120739178G>TCA482146865ACADSc.1068G>T (p.Ala356=)
c.1056G>T (p.Ala352=)
gnomAD v4
12g.120739179A=CA2067555733ACADSc.1069A= (p.Thr357=)
c.1057A= (p.Thr353=)
12g.120739179A>CCA386601703ACADSc.1069A>C (p.Thr357Pro)
c.1057A>C (p.Thr353Pro)
dbSNP gnomAD v4
12g.120739179A>GCA386601704ACADSc.1069A>G (p.Thr357Ala)
c.1057A>G (p.Thr353Ala)
12g.120739179A>TCA386601705ACADSc.1069A>T (p.Thr357Ser)
c.1057A>T (p.Thr353Ser)
12g.120739180C>ACA386601706ACADSc.1070C>A (p.Thr357Asn)
c.1058C>A (p.Thr353Asn)
12g.120739180C=CA2067555734ACADSc.1070C= (p.Thr357=)
c.1058C= (p.Thr353=)
12g.120739180C>GCA386601707ACADSc.1070C>G (p.Thr357Ser)
c.1058C>G (p.Thr353Ser)
dbSNP gnomAD v4
12g.120739180C>TCA386601708ACADSc.1070C>T (p.Thr357Ile)
c.1058C>T (p.Thr353Ile)
12g.120739181C>ACA6831200ACADSc.1071C>A (p.Thr357=)
c.1059C>A (p.Thr353=)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.120739181C=CA2067555735ACADSc.1071C= (p.Thr357=)
c.1059C= (p.Thr353=)
12g.120739181C>GCA482146868ACADSc.1071C>G (p.Thr357=)
c.1059C>G (p.Thr353=)
12g.120739181C>TCA6831201ACADSc.1071C>T (p.Thr357=)
c.1059C>T (p.Thr353=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
12g.120739182G>ACA386601709ACADSc.1072G>A (p.Ala358Thr)
c.1060G>A (p.Ala354Thr)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739182G>CCA386601710ACADSc.1072G>C (p.Ala358Pro)
c.1060G>C (p.Ala354Pro)
12g.120739182G=CA2067555736ACADSc.1072G= (p.Ala358=)
c.1060G= (p.Ala354=)
12g.120739182G>TCA6831202ACADSc.1072G>T (p.Ala358Ser)
c.1060G>T (p.Ala354Ser)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739186_120739192delCA2621370180ACADSc.1076_1082del (p.Ile359ThrfsTer13)
c.1064_1070del (p.Ile355ThrfsTer13)
gnomAD v4
12g.120739183C>ACA386601711ACADSc.1073C>A (p.Ala358Asp)
c.1061C>A (p.Ala354Asp)
12g.120739183C>GCA386601712ACADSc.1073C>G (p.Ala358Gly)
c.1061C>G (p.Ala354Gly)
12g.120739183C>TCA386601713ACADSc.1073C>T (p.Ala358Val)
c.1061C>T (p.Ala354Val)
12g.120739184C>ACA482146871ACADSc.1074C>A (p.Ala358=)
c.1062C>A (p.Ala354=)
12g.120739184C>GCA482146869ACADSc.1074C>G (p.Ala358=)
c.1062C>G (p.Ala354=)
12g.120739184C>TCA482146870ACADSc.1074C>T (p.Ala358=)
c.1062C>T (p.Ala354=)
12g.120739185A=CA2067555737ACADSc.1075A= (p.Ile359=)
c.1063A= (p.Ile355=)
12g.120739185A>CCA386601714ACADSc.1075A>C (p.Ile359Leu)
c.1063A>C (p.Ile355Leu)
12g.120739185A>GCA386601715ACADSc.1075A>G (p.Ile359Val)
c.1063A>G (p.Ile355Val)
dbSNP gnomAD v4
12g.120739185A>TCA386601716ACADSc.1075A>T (p.Ile359Phe)
c.1063A>T (p.Ile355Phe)
12g.120739186T>ACA386601717ACADSc.1076T>A (p.Ile359Asn)
c.1064T>A (p.Ile355Asn)
gnomAD v4
12g.120739186T>CCA386601718ACADSc.1076T>C (p.Ile359Thr)
c.1064T>C (p.Ile355Thr)
gnomAD v4
12g.120739186T>GCA386601719ACADSc.1076T>G (p.Ile359Ser)
c.1064T>G (p.Ile355Ser)
12g.120739187C>ACA482146873ACADSc.1077C>A (p.Ile359=)
c.1065C>A (p.Ile355=)
dbSNP gnomAD v3 gnomAD v4
12g.120739187C=CA2067555738ACADSc.1077C= (p.Ile359=)
c.1065C= (p.Ile355=)
12g.120739187C>GCA386601720ACADSc.1077C>G (p.Ile359Met)
c.1065C>G (p.Ile355Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
12g.120739187C>TCA482146875ACADSc.1077C>T (p.Ile359=)
c.1065C>T (p.Ile355=)
dbSNP gnomAD v2 gnomAD v4
12g.120739188A=CA2067555739ACADSc.1078A= (p.Ser360=)
c.1066A= (p.Ser356=)
12g.120739188A>CCA386601721ACADSc.1078A>C (p.Ser360Arg)
c.1066A>C (p.Ser356Arg)
12g.120739188A>GCA6831203ACADSc.1078A>G (p.Ser360Gly)
c.1066A>G (p.Ser356Gly)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739188A>TCA386601722ACADSc.1078A>T (p.Ser360Cys)
c.1066A>T (p.Ser356Cys)
12g.120739189G>ACA386601723ACADSc.1079G>A (p.Ser360Asn)
c.1067G>A (p.Ser356Asn)
gnomAD v4 COSMIC
12g.120739189G>CCA386601725ACADSc.1079G>C (p.Ser360Thr)
c.1067G>C (p.Ser356Thr)
12g.120739189G>TCA386601724ACADSc.1079G>T (p.Ser360Ile)
c.1067G>T (p.Ser356Ile)
gnomAD v4
12g.120739190C>ACA386601726ACADSc.1080C>A (p.Ser360Arg)
c.1068C>A (p.Ser356Arg)
12g.120739190C>GCA386601727ACADSc.1080C>G (p.Ser360Arg)
c.1068C>G (p.Ser356Arg)
12g.120739190C>TCA482146878ACADSc.1080C>T (p.Ser360=)
c.1068C>T (p.Ser356=)
12g.120739191C>ACA386601728ACADSc.1081C>A (p.His361Asn)
c.1069C>A (p.His357Asn)
12g.120739191C>GCA386601729ACADSc.1081C>G (p.His361Asp)
c.1069C>G (p.His357Asp)
12g.120739191C>TCA386601730ACADSc.1081C>T (p.His361Tyr)
c.1069C>T (p.His357Tyr)
gnomAD v4
12g.120739192A>CCA386601731ACADSc.1082A>C (p.His361Pro)
c.1070A>C (p.His357Pro)
12g.120739192A>GCA386601732ACADSc.1082A>G (p.His361Arg)
c.1070A>G (p.His357Arg)
12g.120739192A>TCA386601733ACADSc.1082A>T (p.His361Leu)
c.1070A>T (p.His357Leu)
12g.120739193C>ACA386601734ACADSc.1083C>A (p.His361Gln)
c.1071C>A (p.His357Gln)
12g.120739193C>GCA386601735ACADSc.1083C>G (p.His361Gln)
c.1071C>G (p.His357Gln)
12g.120739193C>TCA482146880ACADSc.1083C>T (p.His361=)
c.1071C>T (p.His357=)
gnomAD v4
12g.120739194C>ACA386601737ACADSc.1084C>A (p.Gln362Lys)
c.1072C>A (p.Gln358Lys)
gnomAD v4
12g.120739194C=CA2067555740ACADSc.1084C= (p.Gln362=)
c.1072C= (p.Gln358=)
12g.120739194C>GCA386601736ACADSc.1084C>G (p.Gln362Glu)
c.1072C>G (p.Gln358Glu)
ClinVar dbSNP
12g.120739194C>TCA6831204ACADSc.1084C>T (p.Gln362Ter)
c.1072C>T (p.Gln358Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739195A>CCA386601738ACADSc.1085A>C (p.Gln362Pro)
c.1073A>C (p.Gln358Pro)
12g.120739195A>GCA386601739ACADSc.1085A>G (p.Gln362Arg)
c.1073A>G (p.Gln358Arg)
12g.120739195A>TCA386601740ACADSc.1085A>T (p.Gln362Leu)
c.1073A>T (p.Gln358Leu)
gnomAD v4
12g.120739195_120739196delCA912973556ACADSc.1085_1086del (p.Gln362ArgfsTer27)
c.1073_1074del (p.Gln358ArgfsTer27)
12g.120739195_120739196delinsAGCA2067555741ACADSc.1085_1086delinsAG (p.Gln362=)
c.1073_1074delinsAG (p.Gln358=)
12g.120739196G>ACA482146882ACADSc.1086G>A (p.Gln362=)
c.1074G>A (p.Gln358=)
12g.120739196G>CCA386601741ACADSc.1086G>C (p.Gln362His)
c.1074G>C (p.Gln358His)
12g.120739196G>TCA386601742ACADSc.1086G>T (p.Gln362His)
c.1074G>T (p.Gln358His)
12g.120739197delCA658822774ACADSc.1086+1del
c.1074+1del
ClinVar dbSNP gnomAD v4
12g.120739197G>ACA386601743ACADSc.1086+1G>A (n.1086+1G>A)
c.1074+1G>A (n.1074+1G>A)
ClinVar dbSNP
12g.120739197G>CCA386601744ACADSc.1086+1G>C (n.1086+1G>C)
c.1074+1G>C (n.1074+1G>C)
12g.120739197G=CA2067555742ACADSc.1086+1G= (n.1086+1G=)
c.1074+1G= (n.1074+1G=)
12g.120739197G>TCA386601745ACADSc.1086+1G>T (n.1086+1G>T)
c.1074+1G>T (n.1074+1G>T)
ClinVar dbSNP
12g.120739198T>ACA386601746ACADSc.1086+2T>A (n.1086+2T>A)
c.1074+2T>A (n.1074+2T>A)
12g.120739198T>CCA386601747ACADSc.1086+2T>C (n.1086+2T>C)
c.1074+2T>C (n.1074+2T>C)
12g.120739198T>GCA386601748ACADSc.1086+2T>G (n.1086+2T>G)
c.1074+2T>G (n.1074+2T>G)
ClinVar
12g.120739200A>GCA2575321543ACADSc.1086+4A>G (n.1086+4A>G)
c.1074+4A>G (n.1074+4A>G)
12g.120739201G>ACA244495227ACADSc.1086+5G>A (n.1086+5G>A)
c.1074+5G>A (n.1074+5G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739201G=CA2067555743ACADSc.1086+5G= (n.1086+5G=)
c.1074+5G= (n.1074+5G=)
12g.120739207A=CA2067555744ACADSc.1086+11A= (n.1086+11A=)
c.1074+11A= (n.1074+11A=)
12g.120739207A>GCA6831205ACADSc.1086+11A>G (n.1086+11A>G)
c.1074+11A>G (n.1074+11A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739207A>TCA2797705126ACADSc.1086+11A>T (n.1086+11A>T)
c.1074+11A>T (n.1074+11A>T)
12g.120739208C=CA2067555745ACADSc.1086+12C= (n.1086+12C=)
c.1074+12C= (n.1074+12C=)
12g.120739208C>TCA6831206ACADSc.1086+12C>T (n.1086+12C>T)
c.1074+12C>T (n.1074+12C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.120739209A>GCA2621370233ACADSc.1086+13A>G (n.1086+13A>G)
c.1074+13A>G (n.1074+13A>G)
gnomAD v4
12g.120739211T>GCA6831207ACADSc.1086+15T>G (n.1086+15T>G)
c.1074+15T>G (n.1074+15T>G)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.120739211T=CA2067555746ACADSc.1086+15T= (n.1086+15T=)
c.1074+15T= (n.1074+15T=)
12g.120739213A=CA2067555747ACADSc.1086+17A= (n.1086+17A=)
c.1074+17A= (n.1074+17A=)
12g.120739213A>GCA244495261ACADSc.1086+17A>G (n.1086+17A>G)
c.1074+17A>G (n.1074+17A>G)
dbSNP
12g.120739215C>ACA2580085937ACADSc.1086+19C>A (n.1086+19C>A)
c.1074+19C>A (n.1074+19C>A)
ClinVar
12g.120739217C=CA2067555748ACADSc.1086+21C= (n.1086+21C=)
c.1074+21C= (n.1074+21C=)
12g.120739217C>TCA6831208ACADSc.1086+21C>T (n.1086+21C>T)
c.1074+21C>T (n.1074+21C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
12g.120739219G>CCA2575321544ACADSc.1086+23G>C (n.1086+23G>C)
c.1074+23G>C (n.1074+23G>C)
gnomAD v4
12g.120739220_120739221delinsAGCA2067555749ACADSc.1086+24_1086+25delinsAG (n.1086+24_1086+25delinsAG)
c.1074+24_1074+25delinsAG (n.1074+24_1074+25delinsAG)
12g.120739221G>ACA244495273ACADSc.1086+25G>A (n.1086+25G>A)
c.1074+25G>A (n.1074+25G>A)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739221G=CA2067555750ACADSc.1086+25G= (n.1086+25G=)
c.1074+25G= (n.1074+25G=)
12g.120739221G>TCA2621370248ACADSc.1086+25G>T (n.1086+25G>T)
c.1074+25G>T (n.1074+25G>T)
gnomAD v4
12g.120739225dupCA608059972ACADSc.1086+29dup (n.1086+29dup)
c.1074+29dup (n.1074+29dup)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.120739225delCA244495272ACADSc.1086+29del (n.1086+29del)
c.1074+29del (n.1074+29del)
dbSNP
12g.120739222G>ACA2067555752ACADSc.1086+26G>A (n.1086+26G>A)
c.1074+26G>A (n.1074+26G>A)
dbSNP gnomAD v4
12g.120739222G=CA2067555751ACADSc.1086+26G= (n.1086+26G=)
c.1074+26G= (n.1074+26G=)

Number of alleles fetched