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NM_017679.5(BCAS3):c.1157G>T (p.Trp386Leu) AND Inborn genetic diseases

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 16, 2023
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:
RCV004426209.1

Allele description [Variation Report for NM_017679.5(BCAS3):c.1157G>T (p.Trp386Leu)]

NM_017679.5(BCAS3):c.1157G>T (p.Trp386Leu)

Gene:
BCAS3:BCAS3 microtubule associated cell migration factor [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
17q23.2
Genomic location:
Preferred name:
NM_017679.5(BCAS3):c.1157G>T (p.Trp386Leu)
HGVS:
  • NC_000017.11:g.60947288G>T
  • NM_001099432.3:c.1157G>T
  • NM_001320470.3:c.1157G>T
  • NM_001330413.2:c.1157G>T
  • NM_001330414.2:c.1157G>T
  • NM_001353144.2:c.1157G>T
  • NM_001353145.2:c.1157G>T
  • NM_001353146.2:c.1157G>T
  • NM_017679.5:c.1157G>TMANE SELECT
  • NP_001092902.1:p.Trp386Leu
  • NP_001307399.1:p.Trp386Leu
  • NP_001317342.1:p.Trp386Leu
  • NP_001317343.1:p.Trp386Leu
  • NP_001340073.1:p.Trp386Leu
  • NP_001340074.1:p.Trp386Leu
  • NP_001340075.1:p.Trp386Leu
  • NP_060149.3:p.Trp386Leu
  • NC_000017.10:g.59024649G>T
  • NM_001099432.1:c.1157G>T
Protein change:
W386L
Molecular consequence:
  • NM_001099432.3:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001320470.3:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330413.2:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001330414.2:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353144.2:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353145.2:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001353146.2:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_017679.5:c.1157G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Inborn genetic diseases
Identifiers:
MeSH: D030342; MedGen: C0950123

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV004912866Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Uncertain significance
(Dec 16, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Ambry Genetics, SCV004912866.1

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

Description

The c.1157G>T (p.W386L) alteration is located in exon 14 (coding exon 13) of the BCAS3 gene. This alteration results from a G to T substitution at nucleotide position 1157, causing the tryptophan (W) at amino acid position 386 to be replaced by a leucine (L). Based on insufficient or conflicting evidence, the clinical significance of this alteration remains unclear.

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

Last Updated: May 7, 2024