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NM_004999.4(MYO6):c.2665A>G (p.Met889Val) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 14, 2019
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:
RCV001770118.2

Allele description [Variation Report for NM_004999.4(MYO6):c.2665A>G (p.Met889Val)]

NM_004999.4(MYO6):c.2665A>G (p.Met889Val)

Gene:
MYO6:myosin VI [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
6q14.1
Genomic location:
Preferred name:
NM_004999.4(MYO6):c.2665A>G (p.Met889Val)
HGVS:
  • NC_000006.12:g.75890063A>G
  • NG_009934.2:g.145871A>G
  • NM_001300899.2:c.2665A>G
  • NM_001368136.1:c.2665A>G
  • NM_001368137.1:c.2665A>G
  • NM_001368138.1:c.2650A>G
  • NM_001368865.1:c.2665A>G
  • NM_001368866.1:c.2665A>G
  • NM_004999.4:c.2665A>GMANE SELECT
  • NP_001287828.1:p.Met889Val
  • NP_001355065.1:p.Met889Val
  • NP_001355066.1:p.Met889Val
  • NP_001355067.1:p.Met884Val
  • NP_001355794.1:p.Met889Val
  • NP_001355795.1:p.Met889Val
  • NP_004990.3:p.Met889Val
  • LRG_438t1:c.2665A>G
  • LRG_438:g.145871A>G
  • LRG_438p1:p.Met889Val
  • NC_000006.11:g.76599780A>G
  • NG_009934.1:g.145872A>G
  • NM_004999.3:c.2665A>G
  • NR_160538.1:n.2990A>G
Protein change:
M884V
Links:
dbSNP: rs727505098
NCBI 1000 Genomes Browser:
rs727505098
Molecular consequence:
  • NM_001300899.2:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001368136.1:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001368137.1:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001368138.1:c.2650A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001368865.1:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001368866.1:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004999.4:c.2665A>G - missense variant - [Sequence Ontology: SO:0001583]
  • NR_160538.1:n.2990A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: CN517202

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV001993245GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)
Uncertain significance
(Aug 14, 2019)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From GeneDx, SCV001993245.2

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

Description

In silico analysis, which includes protein predictors and evolutionary conservation, supports that this variant does not alter protein structure/function; Has not been previously published as pathogenic or benign to our knowledge

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

Last Updated: Mar 4, 2023