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.4451del (p.Met1484fs)ATMPathogenic/Likely pathogenic11108163360108163360ATAcriteria provided, multiple submitters, no conflictsClinGen:CA658656171
single nucleotide variantNM_000051.4(ATM):c.6586A>T (p.Arg2196Ter)ATMPathogenic/Likely pathogenic11108196050108196050ATcriteria provided, multiple submitters, no conflictsClinGen:CA382554668
single nucleotide variantNM_000051.4(ATM):c.4776+1G>TATMPathogenic/Likely pathogenic11108164205108164205GTcriteria provided, multiple submitters, no conflictsClinGen:CA6265538
DuplicationNM_000051.4(ATM):c.4885dup (p.Val1629fs)ATMPathogenic11108165760108165761TTGcriteria provided, single submitterClinGen:CA658656208
single nucleotide variantNM_000051.4(ATM):c.4909+1G>AATMPathogenic11108165787108165787GAcriteria provided, multiple submitters, no conflictsClinGen:CA6265571
DeletionNM_000051.4(ATM):c.7858del (p.Val2620fs)ATMPathogenic/Likely pathogenic11108203558108203558TGTcriteria provided, multiple submitters, no conflictsClinGen:CA658656302
single nucleotide variantNM_000051.4(ATM):c.5319+2T>CATMPathogenic/Likely pathogenic11108172518108172518TCcriteria provided, multiple submitters, no conflictsClinGen:CA382542858
single nucleotide variantNM_000051.4(ATM):c.5326G>T (p.Glu1776Ter)ATMPathogenic/Likely pathogenic11108173586108173586GTcriteria provided, multiple submitters, no conflictsClinGen:CA382543040
single nucleotide variantNM_000051.4(ATM):c.8011-1G>CATMLikely pathogenic11108205695108205695GCcriteria provided, single submitterClinGen:CA382561831
DuplicationNM_000051.4(ATM):c.5402dup (p.Asn1801fs)ATMPathogenic11108173658108173659GGAcriteria provided, single submitterClinGen:CA658656254