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NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Nov 18, 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:
RCV000788384.2

Allele description [Variation Report for NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)]

NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)

Gene:
MYBPC3:myosin binding protein C3 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
11p11.2
Genomic location:
Preferred name:
NM_000256.3(MYBPC3):c.3232T>C (p.Trp1078Arg)
HGVS:
  • NC_000011.10:g.47333292A>G
  • NG_007667.1:g.24411T>C
  • NM_000256.3:c.3232T>CMANE SELECT
  • NP_000247.2:p.Trp1078Arg
  • LRG_386t1:c.3232T>C
  • LRG_386:g.24411T>C
  • LRG_386p1:p.Trp1078Arg
  • NC_000011.9:g.47354843A>G
Protein change:
W1078R
Links:
dbSNP: rs773543130
NCBI 1000 Genomes Browser:
rs773543130
Molecular consequence:
  • NM_000256.3:c.3232T>C - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000927471Blueprint Genetics
criteria provided, single submitter

(Blueprint Genetics Variant Classification Scheme)
Uncertain significance
(Nov 18, 2017)
germlineclinical testing

Citation Link

Summary from all submissions

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

Details of each submission

From Blueprint Genetics, SCV000927471.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: May 7, 2024