Knowledge base for genomic medicine in Japanese
遺伝性乳がん (ATM/CHEK2)
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
single nucleotide variantNM_000051.4(ATM):c.8988-1G>AATMPathogenic/Likely pathogenic11108236051108236051GAcriteria provided, multiple submitters, no conflictsClinGen:CA348186
single nucleotide variantNM_000051.4(ATM):c.8988-1G>CATMPathogenic11108236051108236051GCcriteria provided, multiple submitters, no conflictsClinGen:CA298332
single nucleotide variantNM_000051.4(ATM):c.8988-2A>CATMLikely pathogenic11108236050108236050ACcriteria provided, single submitter-
single nucleotide variantNM_000051.4(ATM):c.8988-2A>GATMPathogenic/Likely pathogenic11108236050108236050AGcriteria provided, multiple submitters, no conflictsClinGen:CA191650
single nucleotide variantNM_000051.4(ATM):c.8987+1G>CATMPathogenic11108235946108235946GCcriteria provided, single submitterClinGen:CA197313
single nucleotide variantNM_000051.4(ATM):c.8977C>T (p.Arg2993Ter)ATMPathogenic/Likely pathogenic11108235935108235935CTcriteria provided, multiple submitters, no conflictsClinGen:CA194505
DeletionNM_000051.4(ATM):c.8942del (p.His2981fs)ATMPathogenic11108235900108235900CACcriteria provided, multiple submitters, no conflictsClinGen:CA196786
DuplicationNM_000051.4(ATM):c.8925_8928dup (p.Glu2977delinsArgTer)ATMPathogenic11108235882108235883AAAGATcriteria provided, multiple submitters, no conflictsClinGen:CA658656277
IndelNM_000051.4(ATM):c.8918_8929delinsTGT (p.Arg2973_Glu2977delinsMetTer)ATMPathogenic/Likely pathogenic11108235876108235887GGCCGGAAGATGTGTcriteria provided, multiple submitters, no conflictsClinGen:CA16619269
single nucleotide variantNM_000051.4(ATM):c.8911C>T (p.Gln2971Ter)ATMPathogenic/Likely pathogenic11108235869108235869CTcriteria provided, multiple submitters, no conflicts-