Knowledge base for genomic medicine in Japanese
中鎖アシルCoA脱水素酵素欠損症
小児・神経疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_000016.6(ACADM):c.244dup (p.Trp82fs)ACADMPathogenic17619856476198565CCTcriteria provided, multiple submitters, no conflictsClinGen:CA274151
single nucleotide variantNM_000016.6(ACADM):c.233T>C (p.Ile78Thr)ACADMPathogenic17619855476198554TCcriteria provided, multiple submitters, no conflictsClinGen:CA275237,UniProtKB:P11310#VAR_015954
DeletionNM_000016.6(ACADM):c.224del (p.Val75fs)ACADMLikely pathogenic17619854576198545GTGcriteria provided, multiple submitters, no conflictsClinGen:CA16040775
single nucleotide variantNM_000016.6(ACADM):c.218A>G (p.Tyr73Cys)ACADMLikely pathogenic17619853976198539AGcriteria provided, single submitterClinGen:CA16603753
single nucleotide variantNM_000016.6(ACADM):c.217-1G>AACADMPathogenic17619853776198537GAcriteria provided, single submitter-
single nucleotide variantNM_000016.6(ACADM):c.216+2T>GACADMPathogenic17619842876198428TGcriteria provided, multiple submitters, no conflictsClinGen:CA220175
single nucleotide variantNM_000016.6(ACADM):c.216+1G>TACADMLikely pathogenic17619842776198427GTcriteria provided, single submitterClinGen:CA16040774
single nucleotide variantNM_000016.6(ACADM):c.199T>C (p.Tyr67His)ACADMPathogenic/Likely pathogenic17619840976198409TCcriteria provided, multiple submitters, no conflictsClinGen:CA252836,UniProtKB:P11310#VAR_013698,OMIM:607008.0011
DeletionNM_000016.6(ACADM):c.165del (p.Phe55fs)ACADMPathogenic/Likely pathogenic17619837376198373ATAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000016.6(ACADM):c.157C>T (p.Arg53Cys)ACADMPathogenic17619836776198367CTcriteria provided, multiple submitters, no conflictsClinGen:CA220173,UniProtKB:P11310#VAR_000317