U.S. flag

An official website of the United States government

NM_024675.4(PALB2):c.1619A>G (p.Asn540Ser) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 15, 2015
Review status:
1 star out of maximum of 4 stars
criteria provided, single submitter
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:
RCV000486906.1

Allele description [Variation Report for NM_024675.4(PALB2):c.1619A>G (p.Asn540Ser)]

NM_024675.4(PALB2):c.1619A>G (p.Asn540Ser)

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.1619A>G (p.Asn540Ser)
HGVS:
  • NC_000016.10:g.23634927T>C
  • NG_007406.1:g.11431A>G
  • NM_024675.4:c.1619A>GMANE SELECT
  • NP_078951.2:p.Asn540Ser
  • NP_078951.2:p.Asn540Ser
  • LRG_308t1:c.1619A>G
  • LRG_308:g.11431A>G
  • LRG_308p1:p.Asn540Ser
  • NC_000016.9:g.23646248T>C
  • NM_024675.3:c.1619A>G
Protein change:
N540S
Links:
dbSNP: rs1064793609
NCBI 1000 Genomes Browser:
rs1064793609
Molecular consequence:
  • NM_024675.4:c.1619A>G - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

Recent activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000566597GeneDx
criteria provided, single submitter

(GeneDx Variant Classification (06012015))
Uncertain significance
(May 15, 2015)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From GeneDx, SCV000566597.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided

Description

This variant is denoted PALB2 c.1619A>G at the cDNA level, p.Asn540Ser (N540S) at the protein level, and results in the change of an Asparagine to a Serine (AAC>AGC). This variant has not, to our knowledge, been published in the literature as pathogenic or benign. PALB2 Asn540Ser was not observed in approximately 6,500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. Since Asparagine and Serine share similar properties, this is considered a conservative amino acid substitution. PALB2 Asn540Ser occurs at a position that is not conserved, with Serine being the naturally occurring amino acid at this position in one species, and is located in the DNA-binding region (UniProt). In silico analyses predict that this variant is unlikely to alter protein structure or function. Based on currently available information, it is unclear whether PALB2 Asn540Ser is pathogenic or benign. We consider it to be a variant of uncertain significance.

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

Last Updated: Sep 29, 2024