U.S. flag

An official website of the United States government

NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser) AND Autosomal dominant nonsyndromic hearing loss 4A

Germline classification:
Benign (1 submission)
Last evaluated:
May 24, 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:
RCV001129343.12

Allele description [Variation Report for NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser)]

NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser)

Gene:
MYH14:myosin heavy chain 14 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
19q13.33
Genomic location:
Preferred name:
NM_001145809.2(MYH14):c.394G>A (p.Gly132Ser)
HGVS:
  • NC_000019.10:g.50210759G>A
  • NG_011645.1:g.12132G>A
  • NM_001077186.2:c.394G>A
  • NM_001145809.2:c.394G>AMANE SELECT
  • NM_024729.4:c.394G>A
  • NP_001070654.1:p.Gly132Ser
  • NP_001139281.1:p.Gly132Ser
  • NP_079005.3:p.Gly132Ser
  • NP_079005.3:p.Gly132Ser
  • NC_000019.9:g.50714016G>A
  • NM_001145809.1:c.394G>A
  • NM_024729.3:c.394G>A
Protein change:
G132S
Links:
dbSNP: rs199910006
NCBI 1000 Genomes Browser:
rs199910006
Molecular consequence:
  • NM_001077186.2:c.394G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001145809.2:c.394G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_024729.4:c.394G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Autosomal dominant nonsyndromic hearing loss 4A
Synonyms:
Deafness, autosomal dominant 4; Deafness, autosomal dominant 4A
Identifiers:
MONDO: MONDO:0010915; MedGen: C1833503; Orphanet: 90635; OMIM: 600652

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...

Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001288859Illumina Laboratory Services, Illumina
criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)		Benign
(May 24, 2017) 		germlineclinical testing

Citation Link

Help

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, SCV001288859.1

#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 was too high to be consistent with this variant causing disease. Therefore, this variant is classified as benign.

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

Last Updated: Nov 24, 2024