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NM_001079866.2(BCS1L):c.1000G>A (p.Val334Ile) AND not provided

Germline classification:
Conflicting interpretations of pathogenicity (2 submissions)
Last evaluated:
Jan 31, 2024
Review status:
criteria provided, conflicting classifications
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:
RCV000885856.12

Allele description [Variation Report for NM_001079866.2(BCS1L):c.1000G>A (p.Val334Ile)]

NM_001079866.2(BCS1L):c.1000G>A (p.Val334Ile)

Gene:
BCS1L:BCS1 homolog, ubiquinol-cytochrome c reductase complex chaperone [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2q35
Genomic location:
Preferred name:
NM_001079866.2(BCS1L):c.1000G>A (p.Val334Ile)
HGVS:
  • NC_000002.12:g.218662993G>A
  • NG_008018.1:g.8338G>A
  • NG_033099.1:g.1548C>T
  • NM_001079866.2:c.1000G>AMANE SELECT
  • NM_001257342.2:c.1000G>A
  • NM_001257343.2:c.1000G>A
  • NM_001257344.2:c.1000G>A
  • NM_001318836.2:c.640G>A
  • NM_001320717.2:c.1000G>A
  • NM_001371443.1:c.1000G>A
  • NM_001371444.1:c.1000G>A
  • NM_001371446.1:c.1000G>A
  • NM_001371447.1:c.1000G>A
  • NM_001371448.1:c.1000G>A
  • NM_001371449.1:c.1000G>A
  • NM_001371450.1:c.1000G>A
  • NM_001371451.1:c.640G>A
  • NM_001371452.1:c.499G>A
  • NM_001371453.1:c.499G>A
  • NM_001371454.1:c.499G>A
  • NM_001371455.1:c.499G>A
  • NM_001371456.1:c.499G>A
  • NM_001374085.1:c.1000G>A
  • NM_001374086.1:c.499G>A
  • NM_004328.5:c.1000G>A
  • NP_001073335.1:p.Val334Ile
  • NP_001244271.1:p.Val334Ile
  • NP_001244272.1:p.Val334Ile
  • NP_001244273.1:p.Val334Ile
  • NP_001305765.1:p.Val214Ile
  • NP_001307646.1:p.Val334Ile
  • NP_001358372.1:p.Val334Ile
  • NP_001358373.1:p.Val334Ile
  • NP_001358375.1:p.Val334Ile
  • NP_001358376.1:p.Val334Ile
  • NP_001358377.1:p.Val334Ile
  • NP_001358378.1:p.Val334Ile
  • NP_001358379.1:p.Val334Ile
  • NP_001358380.1:p.Val214Ile
  • NP_001358381.1:p.Val167Ile
  • NP_001358382.1:p.Val167Ile
  • NP_001358383.1:p.Val167Ile
  • NP_001358384.1:p.Val167Ile
  • NP_001358385.1:p.Val167Ile
  • NP_001361014.1:p.Val334Ile
  • NP_001361015.1:p.Val167Ile
  • NP_004319.1:p.Val334Ile
  • LRG_539t1:c.1000G>A
  • LRG_539:g.8338G>A
  • NC_000002.11:g.219527716G>A
  • NM_004328.4:c.1000G>A
  • NR_163955.1:n.2007G>A
  • p.Val334Ile
Protein change:
V167I
Links:
dbSNP: rs146731467
NCBI 1000 Genomes Browser:
rs146731467
Molecular consequence:
  • NM_001079866.2:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001257342.2:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001257343.2:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001257344.2:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001318836.2:c.640G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001320717.2:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371443.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371444.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371446.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371447.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371448.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371449.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371450.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371451.1:c.640G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371452.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371453.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371454.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371455.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001371456.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374085.1:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001374086.1:c.499G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004328.5:c.1000G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_163955.1:n.2007G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001029329Invitae
criteria provided, single submitter

(Invitae Variant Classification Sherloc (09022015))
Likely benign
(Jan 31, 2024)
germlineclinical testing

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

SCV001875202GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Uncertain significance
(Aug 23, 2021)
germlineclinical testing

Citation Link

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
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 Invitae, SCV001029329.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

From GeneDx, SCV001875202.1

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

Description

In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: May 19, 2024