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.8416_8418+5delATMLikely pathogenic11108214095108214102TGATGGTGATcriteria provided, multiple submitters, no conflicts-
DeletionNM_000051.4(ATM):c.1066-3_1072delATMLikely pathogenic11108119652108119661ATTTTACAGGTAcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000051.4(ATM):c.3285-2A>GATMPathogenic11108150216108150216AGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000051.4(ATM):c.5496+2T>GATMLikely pathogenic11108173758108173758TGcriteria provided, multiple submitters, no conflicts-
single nucleotide variantNM_000051.4(ATM):c.6453-1G>AATMLikely pathogenic11108192027108192027GAcriteria provided, single submitter-
single nucleotide variantNM_000051.4(ATM):c.6976-1G>AATMPathogenic11108198371108198371GAcriteria provided, single submitter-
DeletionNM_000051.4(ATM):c.8781_8786+2delATMPathogenic11108224601108224608TTCAGAAGGTcriteria provided, single submitter-
DuplicationNC_000011.9:g.(?_108114670)_(108225611_?)dupATMLikely pathogenic11108114670108225611nanacriteria provided, single submitter-
DeletionNC_000011.10:g.(?_108317363)_(108317531_?)delATMPathogenic11108188090108188258nanacriteria provided, single submitter-
DeletionNM_000051.4(ATM):c.1092_1235+363delATMLikely pathogenic11108119686108120192TGGAGATTTCTCAATCTTACACTACTACACAAAGAGAATCTAGTGATTACAGTGTCCCTTGCAAAAGGAAGAAAATAGAACTAGGCTGGGAAGTAATAAAAGATCACCTTCAGAAGTCACAGAATGATTTTGATCTTGTGCCTTGGTAAAGTGTTACCATTTTCTCATTCAGTGTCATTTTAATCTCTTGTATGTTATTTTTCAGAAAACTTTCAGTGGAATCCTTTCATCTCAACCAGAACTAAGTCATTTGTCTACCCCCAAACCTATTACTAGCAAAGGGATATGTGATTGCCATGACAAATGAGATCAATCATTAATGGCTCATTTGCTTGGGCCAAGTGCAGGGCCACCTATTTTAATCATATTGTCATAGCAAGTTAAGAAGGAGGACTGGCTCTCTGATAGGCAATTAGAAGTGTGCACCTCATGGAATTCACTGAATTGTACGCTTCAACAATAGATTTTAGCATACGTAGCACCTTCTAATAGAATTAGGAAGAAGTTATcriteria provided, single submitter-