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NM_006941.4(SOX10):c.122G>T (p.Gly41Val) AND Waardenburg syndrome

Germline classification:
Likely benign (1 submission)
Last evaluated:
Apr 27, 2017
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:
RCV000325156.13

Allele description [Variation Report for NM_006941.4(SOX10):c.122G>T (p.Gly41Val)]

NM_006941.4(SOX10):c.122G>T (p.Gly41Val)

Genes:
POLR2F:RNA polymerase II, I and III subunit F [Gene - OMIM - HGNC]
SOX10:SRY-box transcription factor 10 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
22q13.1
Genomic location:
Preferred name:
NM_006941.4(SOX10):c.122G>T (p.Gly41Val)
HGVS:
  • NC_000022.11:g.37983663C>A
  • NG_007948.1:g.5870G>T
  • NG_148296.1:g.940C>A
  • NM_001301130.2:c.294-2491C>A
  • NM_001301131.2:c.293+16493C>A
  • NM_001363825.1:c.*38+11353C>A
  • NM_006941.4:c.122G>TMANE SELECT
  • NP_008872.1:p.Gly41Val
  • NP_008872.1:p.Gly41Val
  • LRG_271t1:c.122G>T
  • LRG_271:g.5870G>T
  • LRG_271p1:p.Gly41Val
  • NC_000022.10:g.38379670C>A
  • NM_006941.3:c.122G>T
Protein change:
G41V
Links:
dbSNP: rs199750760
NCBI 1000 Genomes Browser:
rs199750760
Molecular consequence:
  • NM_001301130.2:c.294-2491C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001301131.2:c.293+16493C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001363825.1:c.*38+11353C>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_006941.4:c.122G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Waardenburg syndrome
Synonyms:
Van der Hoeve Halbertsma Waardenburg Gualdi Syndrome; Ptosis-Epicanthus Syndrome; Mende Syndrome; See all synonyms [MedGen]
Identifiers:
MONDO: MONDO:0018094; MedGen: C3266898; OMIM: PS193500

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000438627Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)		Likely benign
(Apr 27, 2017) 		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 Illumina Laboratory Services, Illumina, SCV000438627.3

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

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.

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

Last Updated: Apr 20, 2024