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NM_024675.4(PALB2):c.963A>T (p.Leu321Phe) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 25, 2018
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV001030191.1

Allele description [Variation Report for NM_024675.4(PALB2):c.963A>T (p.Leu321Phe)]

NM_024675.4(PALB2):c.963A>T (p.Leu321Phe)

Gene:
PALB2:partner and localizer of BRCA2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
16p12.2
Genomic location:
Preferred name:
NM_024675.4(PALB2):c.963A>T (p.Leu321Phe)
HGVS:
  • NC_000016.10:g.23635583T>A
  • NG_007406.1:g.10775A>T
  • NM_024675.4:c.963A>TMANE SELECT
  • NP_078951.2:p.Leu321Phe
  • LRG_308t1:c.963A>T
  • LRG_308:g.10775A>T
  • NC_000016.9:g.23646904T>A
  • NM_024675.3:c.963A>T
Protein change:
L321F
Links:
dbSNP: rs1967005829
NCBI 1000 Genomes Browser:
rs1967005829
Molecular consequence:
  • NM_024675.4:c.963A>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001193046Leiden Open Variation Database
no assertion criteria provided
Uncertain significance
(Aug 25, 2018) 		germlinecuration

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedcuration

Citations

PubMed

Germline pathogenic variants of 11 breast cancer genes in 7,051 Japanese patients and 11,241 controls.

Momozawa Y, Iwasaki Y, Parsons MT, Kamatani Y, Takahashi A, Tamura C, Katagiri T, Yoshida T, Nakamura S, Sugano K, Miki Y, Hirata M, Matsuda K, Spurdle AB, Kubo M.

Nat Commun. 2018 Oct 4;9(1):4083. doi: 10.1038/s41467-018-06581-8.

PubMed [citation]
PMID:
30287823
PMCID:
PMC6172276

Details of each submission

From Leiden Open Variation Database, SCV001193046.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedcuration PubMed (1)

Description

Curators: Marc Tischkowitz, Arleen D. Auerbach. Submitter to LOVD: Yukihide Momozawa.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Nov 5, 2022