Knowledge base for genomic medicine in Japanese
PALB2変異陽性乳がん・膵臓がん
腫瘍性疾患
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TypeNameGene SymbolClinical SignificanceChromosomeStartStopReference AlleleAlternate AlleleReview StatusOther IDs
(GRCh37)
DeletionNM_024675.4(PALB2):c.1437_1438del (p.Lys480fs)PALB2Pathogenic162364642923646430TTCTcriteria provided, multiple submitters, no conflictsClinGen:CA658683910
DeletionNM_024675.4(PALB2):c.546del (p.Ser183fs)PALB2Pathogenic162364732123647321TGTcriteria provided, single submitterClinGen:CA658683923
single nucleotide variantNM_024675.4(PALB2):c.211+1G>APALB2Likely pathogenic162364917023649170CTcriteria provided, multiple submitters, no conflictsClinGen:CA395139005
single nucleotide variantNM_024675.4(PALB2):c.3166C>T (p.Gln1056Ter)PALB2Pathogenic162362536023625360GAcriteria provided, multiple submitters, no conflictsClinGen:CA279530832
DeletionNM_024675.4(PALB2):c.1914del (p.Phe638fs)PALB2Pathogenic162364156123641561CACcriteria provided, multiple submitters, no conflictsClinGen:CA658683932
DuplicationNM_024675.4(PALB2):c.1276dup (p.Glu426fs)PALB2Pathogenic162364659023646591TTCcriteria provided, single submitterClinGen:CA658683912
single nucleotide variantNM_024675.4(PALB2):c.3350+2C>GPALB2Likely pathogenic162361918323619183GCcriteria provided, multiple submitters, no conflictsClinGen:CA395139182
DeletionNM_024675.4(PALB2):c.1140_1143del (p.Ser380fs)PALB2Pathogenic162364672423646727TAAGATcriteria provided, multiple submitters, no conflictsClinGen:CA621661731
DuplicationNM_024675.4(PALB2):c.1032_1033dup (p.Leu345fs)PALB2Pathogenic162364683323646834AAAGcriteria provided, multiple submitters, no conflictsClinGen:CA658683915
DeletionNM_024675.4(PALB2):c.3228del (p.Cys1078fs)PALB2Pathogenic162361930723619307GAGcriteria provided, single submitterClinGen:CA658683911