NM_007126.5(VCP):c.2242A>T (p.Ser748Cys) AND multiple conditions

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Jul 19, 2022
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:: RCV001210057.8

Allele description [Variation Report for NM_007126.5(VCP):c.2242A>T (p.Ser748Cys)]

NM_007126.5(VCP):c.2242A>T (p.Ser748Cys)

Gene:

VCP:valosin containing protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

9p13.3

Genomic location:

Preferred name:

NM_007126.5(VCP):c.2242A>T (p.Ser748Cys)

HGVS:

NC_000009.12:g.35057449T>A
NG_007887.1:g.20294A>T
NM_001354927.2:c.2107A>T
NM_001354928.2:c.2107A>T
NM_007126.5:c.2242A>TMANE SELECT
NP_001341856.1:p.Ser703Cys
NP_001341857.1:p.Ser703Cys
NP_009057.1:p.Ser748Cys
LRG_657t1:c.2242A>T
LRG_657:g.20294A>T
NC_000009.11:g.35057446T>A
NM_007126.3:c.2242A>T

Protein change:

S703C

Links:

dbSNP: rs1828632660

NCBI 1000 Genomes Browser:

rs1828632660

Molecular consequence:

NM_001354927.2:c.2107A>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001354928.2:c.2107A>T - missense variant - [Sequence Ontology: SO:0001583]
NM_007126.5:c.2242A>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 (FTDALS6)
Synonyms:: Amyotrophic lateral sclerosis 14, with or without frontotemporal dementia; VCP-Related Amyotrophic Lateral Sclerosis; VCP-Related Amyotrophic Lateral Sclerosis/Frontotemporal Dementia
Identifiers:: MONDO: MONDO:0013501; MedGen: C5436279; Orphanet: 275872; Orphanet: 803; OMIM: 613954

Name:: Inclusion body myopathy with Paget disease of bone and frontotemporal dementia
Synonyms:: Inclusion body myopathy with early-onset Paget disease and frontotemporal dementia
Identifiers:: MONDO: MONDO:0000507; MedGen: C1833662; OMIM: PS167320

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001381521	Labcorp Genetics (formerly Invitae), Labcorp	criteria provided, single submitter (Invitae Variant Classification Sherloc (09022015))	Uncertain significance (Jul 19, 2022)	germline	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001381521

Labcorp Genetics (formerly Invitae), Labcorp

criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))

Uncertain significance
(Jul 19, 2022)

germline

clinical testing

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

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

Citations

PubMed

Sherloc: a comprehensive refinement of the ACMG-AMP variant classification criteria.

Nykamp K, Anderson M, Powers M, Garcia J, Herrera B, Ho YY, Kobayashi Y, Patil N, Thusberg J, Westbrook M; Invitae Clinical Genomics Group, Topper S.

Genet Med. 2017 Oct;19(10):1105-1117. doi: 10.1038/gim.2017.37. Epub 2017 May 11. Erratum in: Genet Med. 2020 Jan;22(1):240. doi: 10.1038/s41436-019-0624-9.

PubMed [citation]

PMID:: 28492532
PMCID:: PMC5632818

Details of each submission

From Labcorp Genetics (formerly Invitae), Labcorp, SCV001381521.5

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

Description

This variant has not been reported in the literature in individuals affected with VCP-related conditions. ClinVar contains an entry for this variant (Variation ID: 940463). This variant is not present in population databases (gnomAD no frequency). This sequence change replaces serine, which is neutral and polar, with cysteine, which is neutral and slightly polar, at codon 748 of the VCP protein (p.Ser748Cys). In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance. Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Not Available"; PolyPhen-2: "Possibly Damaging"; Align-GVGD: "Not Available").

#	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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