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)
DeletionNM_000051.4(ATM):c.6729_6730del (p.Glu2245fs)ATMPathogenic11108196192108196193CAACcriteria provided, single submitterClinGen:CA16613193
DeletionNC_000011.10:g.(?_108243953)_(108369099_?)delATMPathogenic11108114680108239826nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_108297287)_(108335961_?)delATMPathogenic11108168014108206688nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_108325310)_(108369099_?)delATMPathogenic11108196037108239826nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_108327645)_(108331557_?)delATMLikely pathogenic11108198372108202284nanacriteria provided, single submitter-
single nucleotide variantNM_000051.4(ATM):c.8880G>A (p.Trp2960Ter)ATMPathogenic11108235838108235838GAcriteria provided, multiple submitters, no conflictsClinGen:CA16613231
DeletionNM_000051.4(ATM):c.1783_1802+91delATMLikely pathogenic11108122738108122848AAGTGCCTCCAATTCTTCACAGGTAATTTAAGTTCATTAGCATGCTGCTGTTTTTTTTGTTTGTTTTATCAGGCTCTCTCCACTTATTTGATGCCAGATGGCTTTATTTTATAcriteria provided, multiple submitters, no conflictsClinGen:CA16613267
DeletionNC_000011.10:g.(?_108280995)_(108289801_?)delATMPathogenic11108151722108160528nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_108343222)_(108369099_?)delATMPathogenic11108213949108239826nanacriteria provided, single submitter-
DeletionNM_000051.4(ATM):c.710del (p.Thr237fs)ATMPathogenic11108115562108115562ACAcriteria provided, multiple submitters, no conflictsClinGen:CA16613298