Knowledge base for genomic medicine in Japanese
原発性免疫不全症候群
小児・神経疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_000051.4(ATM):c.689del (p.Asn230fs)ATMPathogenic/Likely pathogenic11108115539108115539TATcriteria provided, multiple submitters, no conflictsClinGen:CA16043454
single nucleotide variantNM_000051.4(ATM):c.497-1G>AATMLikely pathogenic11108114679108114679GAcriteria provided, single submitterClinVar:424841,ClinGen:CA6264624
single nucleotide variantNM_000051.4(ATM):c.1236-2A>TATMPathogenic11108121426108121426ATcriteria provided, multiple submitters, no conflictsClinVar:424841,ClinGen:CA6264792
single nucleotide variantNM_000051.4(ATM):c.4106C>A (p.Ser1369Ter)ATMPathogenic/Likely pathogenic11108158439108158439CAcriteria provided, multiple submitters, no conflictsClinGen:CA16606070
single nucleotide variantNM_000051.4(ATM):c.6096-2A>GATMPathogenic/Likely pathogenic11108186736108186736AGcriteria provided, multiple submitters, no conflictsClinGen:CA501172
single nucleotide variantNM_000051.4(ATM):c.2115C>G (p.Tyr705Ter)ATMPathogenic/Likely pathogenic11108124757108124757CGcriteria provided, multiple submitters, no conflictsClinGen:CA16606161
single nucleotide variantNM_000051.4(ATM):c.901+1G>CATMPathogenic11108115754108115754GCcriteria provided, multiple submitters, no conflictsClinGen:CA16606776
single nucleotide variantNM_000051.4(ATM):c.8641C>T (p.Gln2881Ter)ATMPathogenic11108218062108218062CTcriteria provided, multiple submitters, no conflictsClinGen:CA16606855
DeletionNC_000011.10:g.(?_108222832)_(108369099_?)delATMPathogenic11108093559108239826nanacriteria provided, single submitter-
DeletionNM_000051.4(ATM):c.1212_1213del (p.Gln404_Asn405insTer)ATMPathogenic11108119805108119806CAGCcriteria provided, multiple submitters, no conflictsClinGen:CA16612981