U.S. flag

An official website of the United States government

NM_001127649.3(PEX26):c.208G>T (p.Val70Leu) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
May 29, 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:
RCV001321237.6

Allele description [Variation Report for NM_001127649.3(PEX26):c.208G>T (p.Val70Leu)]

NM_001127649.3(PEX26):c.208G>T (p.Val70Leu)

Gene:
PEX26:peroxisomal biogenesis factor 26 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q11.21
Genomic location:
Preferred name:
NM_001127649.3(PEX26):c.208G>T (p.Val70Leu)
HGVS:
  • NC_000022.11:g.18078584G>T
  • NG_008339.1:g.5665G>T
  • NM_001127649.3:c.208G>TMANE SELECT
  • NM_001199319.2:c.208G>T
  • NM_017929.6:c.208G>T
  • NP_001121121.1:p.Val70Leu
  • NP_001186248.1:p.Val70Leu
  • NP_060399.1:p.Val70Leu
  • NC_000022.10:g.18561350G>T
  • NM_017929.5:c.208G>T
Protein change:
V70L
Links:
dbSNP: rs766581207
NCBI 1000 Genomes Browser:
rs766581207
Molecular consequence:
  • NM_001127649.3:c.208G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001199319.2:c.208G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_017929.6:c.208G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Peroxisome biogenesis disorder 7A (Zellweger)
Synonyms:
Peroxisome biogenesis disorder 7A
Identifiers:
MONDO: MONDO:0013938; MedGen: C3888385; Orphanet: 912; OMIM: 614872
Name:
Peroxisome biogenesis disorder 7B (PBD7B)
Identifiers:
MONDO: MONDO:0013939; MedGen: C3553951; Orphanet: 44; OMIM: 614873

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001512059Labcorp Genetics (formerly Invitae), Labcorp
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))		Uncertain significance
(May 29, 2022) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical 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, SCV001512059.3

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This sequence change replaces valine, which is neutral and non-polar, with leucine, which is neutral and non-polar, at codon 70 of the PEX26 protein (p.Val70Leu). The frequency data for this variant in the population databases is considered unreliable, as metrics indicate poor data quality at this position in the gnomAD database. This variant has not been reported in the literature in individuals affected with PEX26-related conditions. ClinVar contains an entry for this variant (Variation ID: 340752). Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. 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.

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

Last Updated: Oct 13, 2024