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NM_000260.4(MYO7A):c.2094+1G>C AND Rare genetic deafness

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Nov 4, 2008
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:
RCV000036076.5

Allele description [Variation Report for NM_000260.4(MYO7A):c.2094+1G>C]

NM_000260.4(MYO7A):c.2094+1G>C

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.2094+1G>C
HGVS:
  • NC_000011.10:g.77174915G>C
  • NG_009086.2:g.51670G>C
  • NM_000260.4:c.2094+1G>CMANE SELECT
  • NM_001127180.2:c.2094+1G>C
  • NM_001369365.1:c.2061+1G>C
  • LRG_1420t1:c.2094+1G>C
  • LRG_1420:g.51670G>C
  • NC_000011.9:g.76885961G>C
  • NM_000260.3:c.2094+1G>C
  • c.2094+1G>C
Links:
dbSNP: rs111033404
NCBI 1000 Genomes Browser:
rs111033404
Molecular consequence:
  • NM_000260.4:c.2094+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001127180.2:c.2094+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
  • NM_001369365.1:c.2061+1G>C - splice donor variant - [Sequence Ontology: SO:0001575]
Observations:
1

Condition(s)

Name:
Rare genetic deafness
Identifiers:
MedGen: C5680250; Orphanet: 96210

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000059728Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine
criteria provided, single submitter

(LMM Criteria)		Likely pathogenic
(Nov 4, 2008) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided21not providednot providednot providedclinical testing

Citations

PubMed

A systematic approach to assessing the clinical significance of genetic variants.

Duzkale H, Shen J, McLaughlin H, Alfares A, Kelly MA, Pugh TJ, Funke BH, Rehm HL, Lebo MS.

Clin Genet. 2013 Nov;84(5):453-63. doi: 10.1111/cge.12257.

PubMed [citation]
PMID:
24033266
PMCID:
PMC3995020

Details of each submission

From Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine, SCV000059728.6

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided2not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided2not provided1not provided

Last Updated: Dec 24, 2023