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NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile) AND Autosomal recessive nonsyndromic hearing loss 2

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:
RCV000289903.13

Allele description [Variation Report for NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)]

NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)

Gene:
MYO7A:myosin VIIA [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11q13.5
Genomic location:
Preferred name:
NM_000260.4(MYO7A):c.2035G>A (p.Val679Ile)
HGVS:
  • NC_000011.10:g.77174855G>A
  • NG_009086.2:g.51610G>A
  • NM_000260.4:c.2035G>AMANE SELECT
  • NM_001127180.2:c.2035G>A
  • NM_001369365.1:c.2002G>A
  • NP_000251.3:p.Val679Ile
  • NP_001120652.1:p.Val679Ile
  • NP_001356294.1:p.Val668Ile
  • LRG_1420t1:c.2035G>A
  • LRG_1420:g.51610G>A
  • LRG_1420p1:p.Val679Ile
  • NC_000011.9:g.76885901G>A
  • NG_009086.1:g.51592G>A
  • NM_000260.3:c.2035G>A
  • Q13402:p.Val679Ile
  • c.2035G>A
Protein change:
V668I
Links:
UniProtKB: Q13402#VAR_056188; dbSNP: rs35641839
NCBI 1000 Genomes Browser:
rs35641839
Molecular consequence:
  • NM_000260.4:c.2035G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127180.2:c.2035G>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369365.1:c.2002G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Autosomal recessive nonsyndromic hearing loss 2
Synonyms:
NEUROSENSORY NONSYNDROMIC RECESSIVE DEAFNESS 2; Deafness, autosomal recessive 2
Identifiers:
MONDO: MONDO:0010807; MedGen: C1838701; Orphanet: 90636; OMIM: 600060

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000374266Illumina 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, SCV000374266.3

#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: Oct 26, 2024