Knowledge base for genomic medicine in Japanese
MUTYH関連ポリポーシス
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_001048174.2(MUTYH):c.1407T>G (p.Tyr469Ter)MUTYHLikely pathogenic14579621545796215ACcriteria provided, single submitterClinGen:CA16617152
DuplicationNM_001048174.2(MUTYH):c.1363dup (p.Thr455fs)MUTYHPathogenic/Likely pathogenic14579688245796883GGTcriteria provided, multiple submitters, no conflictsClinGen:CA16617154
DeletionNM_001048174.2(MUTYH):c.1237del (p.Glu413fs)MUTYHPathogenic/Likely pathogenic14579709445797094TCTcriteria provided, multiple submitters, no conflictsClinGen:CA16617155
single nucleotide variantNM_001048174.2(MUTYH):c.1102G>A (p.Gly368Ser)MUTYHLikely pathogenic14579733345797333CTcriteria provided, single submitterClinGen:CA16617156
IndelNM_001048174.2(MUTYH):c.632_637delinsCAGCTGCT (p.Val211fs)MUTYHPathogenic14579813045798135GTGCTAAGCAGCTGcriteria provided, multiple submitters, no conflictsClinGen:CA16617162
single nucleotide variantNM_001048174.2(MUTYH):c.604C>T (p.Gln202Ter)MUTYHPathogenic/Likely pathogenic14579824845798248GAcriteria provided, multiple submitters, no conflictsClinGen:CA16617164
DeletionNM_001128425.2(MUTYH):c.200del (p.Gly67fs)MUTYHPathogenic/Likely pathogenic14579923345799233GCGcriteria provided, multiple submitters, no conflictsClinGen:CA055834
single nucleotide variantNM_001128425.2(MUTYH):c.35G>A (p.Trp12Ter)MUTYHPathogenic/Likely pathogenic14580589245805892CTcriteria provided, multiple submitters, no conflictsClinGen:CA16617170
single nucleotide variantNM_001048174.2(MUTYH):c.1041T>A (p.Cys347Ter)MUTYHPathogenic14579739445797394ATcriteria provided, single submitterClinGen:CA340133475
DeletionNC_000001.11:g.(?_45329306)_(45333324_?)delMUTYHPathogenic14579497845798996nanacriteria provided, single submitter-