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NM_006514.4(SCN10A):c.3263C>T (p.Thr1088Met) AND Cardiovascular phenotype

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 15, 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:
RCV004452883.1

Allele description [Variation Report for NM_006514.4(SCN10A):c.3263C>T (p.Thr1088Met)]

NM_006514.4(SCN10A):c.3263C>T (p.Thr1088Met)

Genes:
LOC110121288:VISTA enhancer hs2268 [Gene]
SCN10A:sodium voltage-gated channel alpha subunit 10 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3p22.2
Genomic location:
Preferred name:
NM_006514.4(SCN10A):c.3263C>T (p.Thr1088Met)
HGVS:
  • NC_000003.12:g.38723519G>A
  • NG_031891.2:g.75492C>T
  • NG_031891.3:g.97698C>T
  • NG_053903.1:g.1484G>A
  • NM_001293306.2:c.3260C>T
  • NM_001293307.2:c.2969C>T
  • NM_006514.4:c.3263C>TMANE SELECT
  • NP_001280235.2:p.Thr1087Met
  • NP_001280236.2:p.Thr990Met
  • NP_006505.4:p.Thr1088Met
  • NC_000003.11:g.38765010G>A
  • NM_006514.2:c.3263C>T
Protein change:
T1087M
Molecular consequence:
  • NM_001293306.2:c.3260C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001293307.2:c.2969C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_006514.4:c.3263C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV004945191Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)
Uncertain significance
(Dec 15, 2023)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV004945191.1

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

Description

The c.3263C>T (p.T1088M) alteration is located in exon 18 (coding exon 18) of the SCN10A gene. This alteration results from a C to T substitution at nucleotide position 3263, causing the threonine (T) at amino acid position 1088 to be replaced by a methionine (M). 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