Knowledge base for genomic medicine in Japanese
海綿状血管腫
小児・神経疾患
Excelでダウンロード
表のタイトル行が青色の項目は、クリックすることでソートすることができます。
TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DuplicationNM_194454.3(KRIT1):c.1470dup (p.Leu491fs)KRIT1Likely pathogenic79185130891851309GGTcriteria provided, single submitter-
DuplicationNM_194454.3(KRIT1):c.1421_1422dup (p.Lys475fs)KRIT1Likely pathogenic79185135691851357TTGAcriteria provided, single submitter-
single nucleotide variantNM_194454.3(KRIT1):c.1412-2A>CKRIT1Pathogenic79185136991851369TGcriteria provided, multiple submitters, no conflicts-
DuplicationNM_194454.3(KRIT1):c.1406dup (p.Asn469fs)KRIT1Likely pathogenic79185214091852141GGTcriteria provided, single submitter-
single nucleotide variantNM_194454.3(KRIT1):c.1391G>A (p.Trp464Ter)KRIT1Pathogenic79185215691852156CTcriteria provided, single submitter-
single nucleotide variantNM_194454.3(KRIT1):c.1372C>T (p.Gln458Ter)KRIT1Pathogenic/Likely pathogenic79185217591852175GAcriteria provided, multiple submitters, no conflicts-
DeletionNM_194454.3(KRIT1):c.1355_1359del (p.Arg452fs)KRIT1Likely pathogenic79185218891852192AGAGACAcriteria provided, single submitter-
DuplicationNM_194454.3(KRIT1):c.1358dup (p.Ser454fs)KRIT1Likely pathogenic79185218891852189GGAcriteria provided, single submitter-
IndelNM_194454.3(KRIT1):c.1263_1267delinsTGTA (p.Lys421fs)KRIT1Likely pathogenic79185228091852284GAACTTACAcriteria provided, single submitter-
single nucleotide variantNM_194454.3(KRIT1):c.1255-1G>AKRIT1Pathogenic79185229391852293CTcriteria provided, multiple submitters, no conflicts-