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.964_968del (p.Glu322fs)ATMPathogenic11108117751108117755AATGAGAcriteria provided, multiple submitters, no conflictsClinGen:CA658656195
DuplicationNM_000051.4(ATM):c.441dup (p.Asp148fs)ATMPathogenic11108106503108106504CCAcriteria provided, multiple submitters, no conflictsClinGen:CA658656155
DuplicationNM_000051.4(ATM):c.442dup (p.Asp148fs)ATMPathogenic11108106506108106507AAGcriteria provided, multiple submitters, no conflictsClinGen:CA658656156
single nucleotide variantNM_000051.4(ATM):c.1003G>T (p.Gly335Ter)ATMPathogenic/Likely pathogenic11108117792108117792GTcriteria provided, multiple submitters, no conflictsClinGen:CA382531372
single nucleotide variantNM_000051.4(ATM):c.1178G>A (p.Trp393Ter)ATMPathogenic11108119772108119772GAcriteria provided, multiple submitters, no conflictsClinGen:CA382532540
DeletionNM_000051.4(ATM):c.1464del (p.Trp488fs)ATMPathogenic11108121655108121655TGTcriteria provided, single submitterClinGen:CA658656146
single nucleotide variantNM_000051.4(ATM):c.73-1G>AATMPathogenic/Likely pathogenic11108098502108098502GAcriteria provided, multiple submitters, no conflictsClinGen:CA382519448
DuplicationNM_000051.4(ATM):c.2749dup (p.Ser917fs)ATMPathogenic11108139246108139247GGTcriteria provided, multiple submitters, no conflictsClinGen:CA658656142
single nucleotide variantNM_000051.4(ATM):c.2838+1G>TATMLikely pathogenic11108139337108139337GTcriteria provided, multiple submitters, no conflictsClinGen:CA382545873
single nucleotide variantNM_000051.4(ATM):c.186-1G>AATMLikely pathogenic11108099904108099904GAcriteria provided, multiple submitters, no conflictsClinGen:CA382520987