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NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu) AND not provided

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Feb 23, 2023
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:
RCV000158668.4

Allele description [Variation Report for NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu)]

NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu)

Genes:
LOC126861897:BRD4-independent group 4 enhancer GRCh37_chr14:23884455-23885654 [Gene]
MYH7:myosin heavy chain 7 [Gene - OMIM - HGNC]
MHRT:myosin heavy chain associated RNA transcript [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
14q11.2
Genomic location:
Preferred name:
NM_000257.4(MYH7):c.4709C>A (p.Ala1570Glu)
Other names:
p.A1570E:GCA>GAA
HGVS:
  • NC_000014.9:g.23416248G>T
  • NG_007884.1:g.24414C>A
  • NM_000257.4:c.4709C>AMANE SELECT
  • NP_000248.2:p.Ala1570Glu
  • LRG_384t1:c.4709C>A
  • LRG_384:g.24414C>A
  • NC_000014.8:g.23885457G>T
  • NM_000257.2:c.4709C>A
  • NM_000257.3:c.4709C>A
  • NR_126491.1:n.509G>T
Protein change:
A1570E
Links:
dbSNP: rs730880807
NCBI 1000 Genomes Browser:
rs730880807
Molecular consequence:
  • NM_000257.4:c.4709C>A - missense variant - [Sequence Ontology: SO:0001583]
  • NR_126491.1:n.509G>T - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000208603GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Feb 23, 2023) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From GeneDx, SCV000208603.14

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

Description

Not observed at a significant frequency in large population cohorts (gnomAD); In silico analysis supports that this missense variant does not alter protein structure/function; Has not been previously published in association with cardiomyopathy to our knowledge; This variant is associated with the following publications: (PMID: 34542152)

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

Last Updated: Sep 29, 2024