NM_024675.4(PALB2):c.1958G>T (p.Cys653Phe) AND PALB2-related disorder

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Mar 1, 2024
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:: RCV004527779.2

Allele description [Variation Report for NM_024675.4(PALB2):c.1958G>T (p.Cys653Phe)]

NM_024675.4(PALB2):c.1958G>T (p.Cys653Phe)

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.1958G>T (p.Cys653Phe)

HGVS:

NC_000016.10:g.23630196C>A
NG_007406.1:g.16162G>T
NM_024675.4:c.1958G>TMANE SELECT
NP_078951.2:p.Cys653Phe
NP_078951.2:p.Cys653Phe
LRG_308t1:c.1958G>T
LRG_308:g.16162G>T
LRG_308p1:p.Cys653Phe
NC_000016.9:g.23641517C>A
NM_024675.3:c.1958G>T

Protein change:

C653F

Links:

dbSNP: rs771246748

NCBI 1000 Genomes Browser:

rs771246748

Molecular consequence:

NM_024675.4:c.1958G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: PALB2-related disorder
Synonyms:: PALB2-related condition; PALB2-Related Disorders
Identifiers:

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV004103252	PreventionGenetics, part of Exact Sciences	no assertion criteria provided	Uncertain significance (Mar 1, 2024)	germline	clinical testing

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV004103252

PreventionGenetics, part of Exact Sciences

no assertion criteria provided

Uncertain significance
(Mar 1, 2024)

germline

clinical testing

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From PreventionGenetics, part of Exact Sciences, SCV004103252.3

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The PALB2 c.1958G>T variant is predicted to result in the amino acid substitution p.Cys653Phe. To our knowledge, this variant has not been reported in the literature or in a large population database (http://gnomad.broadinstitute.org), indicating this variant is rare. This variant has been interpreted by multiple laboratories in ClinVar as uncertain (https://preview.ncbi.nlm.nih.gov/clinvar/variation/630507/). At this time, the clinical significance of this variant is uncertain due to the absence of conclusive functional and genetic evidence.

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 3, 2024

ClinVar

Relating variation to medicine