NM_024675.4(PALB2):c.2238A>G (p.Ala746=) AND Hereditary cancer-predisposing syndrome

Germline classification:: Likely benign (1 submission)
Last evaluated:: Mar 28, 2018
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:: RCV001014874.4

Allele description [Variation Report for NM_024675.4(PALB2):c.2238A>G (p.Ala746=)]

NM_024675.4(PALB2):c.2238A>G (p.Ala746=)

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.2238A>G (p.Ala746=)

HGVS:

NC_000016.10:g.23629916T>C
NG_007406.1:g.16442A>G
NM_024675.4:c.2238A>GMANE SELECT
NP_078951.2:p.Ala746=
LRG_308t1:c.2238A>G
LRG_308:g.16442A>G
NC_000016.9:g.23641237T>C
NC_000016.9:g.23641237T>C
NM_024675.3:c.2238A>G

Links:

dbSNP: rs1597089677

NCBI 1000 Genomes Browser:

rs1597089677

Molecular consequence:

NM_024675.4:c.2238A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:: Hereditary cancer-predisposing syndrome
Synonyms:: Neoplastic Syndromes, Hereditary; Tumor predisposition; Cancer predisposition; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0015356; MeSH: D009386; MedGen: C0027672

Recent activity

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SCV000078163 (1)
ClinVar
Homo sapiens synaptotagmin like 5 (SYTL5), transcript variant 3, mRNA
Homo sapiens synaptotagmin like 5 (SYTL5), transcript variant 3, mRNA
gi|254039647|ref|NM_001163334.1|

Nucleotide
uncharacterized protein LOC111480421 isoform X1 [Cucurbita maxima]
uncharacterized protein LOC111480421 isoform X1 [Cucurbita maxima]
gi|1280995077|ref|XP_022981213.1|

Protein

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001175639	Ambry Genetics	criteria provided, single submitter (Ambry Variant Classification Scheme 2023)	Likely benign (Mar 28, 2018)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001175639

Ambry Genetics

criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)

Likely benign
(Mar 28, 2018)

germline

clinical testing

Citation Link

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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 Ambry Genetics, SCV001175639.4

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

#	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: Sep 29, 2024

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