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NM_006514.4(SCN10A):c.2910C>T (p.Ser970=) AND Cardiovascular phenotype

Germline classification:
Likely benign (1 submission)
Last evaluated:
Nov 30, 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:
RCV004371885.1

Allele description [Variation Report for NM_006514.4(SCN10A):c.2910C>T (p.Ser970=)]

NM_006514.4(SCN10A):c.2910C>T (p.Ser970=)

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.2910C>T (p.Ser970=)
HGVS:
  • NC_000003.12:g.38726783G>A
  • NG_031891.2:g.72228C>T
  • NG_031891.3:g.94434C>T
  • NG_053903.1:g.4748G>A
  • NM_001293306.2:c.2910C>T
  • NM_001293307.2:c.2616C>T
  • NM_006514.2:c.2910C>T
  • NM_006514.4:c.2910C>TMANE SELECT
  • NP_001280235.2:p.Ser970=
  • NP_001280236.2:p.Ser872=
  • NP_006505.4:p.Ser970=
  • NC_000003.11:g.38768274G>A
Molecular consequence:
  • NM_001293306.2:c.2910C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001293307.2:c.2616C>T - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_006514.4:c.2910C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005024927Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Likely benign
(Nov 30, 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, SCV005024927.1

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

Description

This alteration is classified as likely benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Sep 29, 2024