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)
DuplicationNM_000051.4(ATM):c.5894_5900dup (p.Met1967fs)ATMPathogenic/Likely pathogenic11108181017108181018AAAAAGTATcriteria provided, multiple submitters, no conflictsClinGen:CA16619205
DeletionNM_000051.4(ATM):c.6059del (p.Gly2020fs)ATMPathogenic11108186601108186601TGTcriteria provided, single submitterClinGen:CA16619207
single nucleotide variantNM_000051.4(ATM):c.6238T>G (p.Tyr2080Asp)ATMLikely pathogenic11108188139108188139TGcriteria provided, multiple submitters, no conflictsClinGen:CA16619210
DuplicationNM_000051.4(ATM):c.6730dup (p.Arg2244fs)ATMPathogenic/Likely pathogenic11108196191108196192CCAcriteria provided, multiple submitters, no conflictsClinGen:CA16619219
IndelNM_000051.4(ATM):c.6736_6755delinsCA (p.Cys2246_Thr2252delinsHis)ATMLikely pathogenic11108196200108196219TGTATTAAGGACATTCTCACCAcriteria provided, single submitterClinGen:CA16619220
DeletionNM_000051.4(ATM):c.6754del (p.Thr2252fs)ATMPathogenic11108196218108196218CACcriteria provided, multiple submitters, no conflictsClinGen:CA16619221
DeletionNM_000051.4(ATM):c.6920_6923del (p.Leu2307fs)ATMPathogenic11108196896108196899TCTTGTcriteria provided, multiple submitters, no conflictsClinGen:CA16619223
DuplicationNM_000051.4(ATM):c.7347dup (p.Leu2450fs)ATMLikely pathogenic11108200978108200979GGAcriteria provided, single submitterClinGen:CA16619230
DeletionNM_000051.4(ATM):c.7391_7412del (p.Cys2464fs)ATMLikely pathogenic11108201021108201042TTATGTAAAGCAGTTGAAAATTATcriteria provided, single submitterClinGen:CA16619232
single nucleotide variantNM_000051.4(ATM):c.7630-2A>GATMPathogenic/Likely pathogenic11108202604108202604AGcriteria provided, multiple submitters, no conflictsClinGen:CA16619236