Knowledge base for genomic medicine in Japanese
ポリメラーゼ校正関連ポリポーシス
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_006231.4(POLE):c.3071del (p.Met1024fs)POLEPathogenic12133236085133236085CACcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.4231_4232del (p.Ile1411fs)POLEPathogenic12133220481133220482GATGcriteria provided, single submitter-
DuplicationNM_006231.4(POLE):c.4552-1dupPOLEPathogenic12133219581133219582AACcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.4593_4611del (p.Ala1532fs)POLEPathogenic12133219523133219541GGAGGAGGCCGTGCTCTGCTGcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.4959del (p.His1654fs)POLEPathogenic12133218977133218977GAGcriteria provided, single submitter-
single nucleotide variantNM_006231.4(POLE):c.5245G>T (p.Glu1749Ter)POLEPathogenic12133218366133218366CAcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.5336del (p.Pro1779fs)POLEPathogenic12133218275133218275CGCcriteria provided, single submitter-
single nucleotide variantNM_006231.4(POLE):c.5658C>A (p.Tyr1886Ter)POLEPathogenic12133214620133214620GTcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.5783_5784del (p.Lys1928fs)POLEPathogenic12133212505133212506CTTCcriteria provided, single submitter-
DeletionNM_006231.4(POLE):c.6023del (p.Tyr2008fs)POLEPathogenic12133209363133209363GTGcriteria provided, single submitter-