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NM_000260.4(MYO7A):c.3560G>T (p.Ser1187Ile) AND Autosomal dominant nonsyndromic hearing loss 11

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Dec 21, 2018
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:
RCV001334333.1

Allele description [Variation Report for NM_000260.4(MYO7A):c.3560G>T (p.Ser1187Ile)]

NM_000260.4(MYO7A):c.3560G>T (p.Ser1187Ile)

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.3560G>T (p.Ser1187Ile)
HGVS:
  • NC_000011.10:g.77189400G>T
  • NG_009086.2:g.66155G>T
  • NM_000260.4:c.3560G>TMANE SELECT
  • NM_001127180.2:c.3560G>T
  • NM_001369365.1:c.3527G>T
  • NP_000251.3:p.Ser1187Ile
  • NP_001120652.1:p.Ser1187Ile
  • NP_001356294.1:p.Ser1176Ile
  • LRG_1420t1:c.3560G>T
  • LRG_1420:g.66155G>T
  • LRG_1420p1:p.Ser1187Ile
  • NC_000011.9:g.76900445G>T
  • NG_009086.1:g.66136G>T
  • NM_000260.3:c.3560G>T
Protein change:
S1176I
Links:
dbSNP: rs1555090314
NCBI 1000 Genomes Browser:
rs1555090314
Molecular consequence:
  • NM_000260.4:c.3560G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001127180.2:c.3560G>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001369365.1:c.3527G>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Autosomal dominant nonsyndromic hearing loss 11
Synonyms:
Deafness, autosomal dominant 11
Identifiers:
MONDO: MONDO:0011032; MedGen: C1832475; Orphanet: 90635; OMIM: 601317

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001527146Baylor Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Dec 21, 2018) 		maternalclinical testing

PubMed (1)
[See all records that cite this PMID]

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Baylor Genetics, SCV001527146.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

This variant was determined to be of uncertain significance according to ACMG Guidelines, 2015 [PMID:25741868].

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

Last Updated: Jun 17, 2024