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NM_000257.4(MYH7):c.4716C>T (p.Ile1572=) AND Cardiovascular phenotype

Germline classification:
Benign (1 submission)
Last evaluated:
Jun 25, 2015
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:
RCV000247901.12

Allele description [Variation Report for NM_000257.4(MYH7):c.4716C>T (p.Ile1572=)]

NM_000257.4(MYH7):c.4716C>T (p.Ile1572=)

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.4716C>T (p.Ile1572=)
Other names:
NM_000257.3(MYH7):c.4716C>T
HGVS:
  • NC_000014.9:g.23416241G>A
  • NG_007884.1:g.24421C>T
  • NM_000257.4:c.4716C>TMANE SELECT
  • NP_000248.2:p.Ile1572=
  • LRG_384t1:c.4716C>T
  • LRG_384:g.24421C>T
  • NC_000014.8:g.23885450G>A
  • NM_000257.2:c.4716C>T
  • NM_000257.3:c.4716C>T
  • NR_126491.1:n.502G>A
  • c.4716C>T
  • p.Ile1572Ile
Links:
dbSNP: rs7140196
NCBI 1000 Genomes Browser:
rs7140196
Molecular consequence:
  • NR_126491.1:n.502G>A - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_000257.4:c.4716C>T - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Cardiovascular phenotype
Identifiers:
MedGen: CN230736

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Assertion and evidence details

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Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000318784Ambry Genetics
criteria provided, single submitter

(Ambry Variant Classification Scheme 2023)		Benign
(Jun 25, 2015) 		germlineclinical testing

Citation Link

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Summary from all submissions

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

Details of each submission

From Ambry Genetics, SCV000318784.7

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

Description

This alteration is classified as benign based on a combination of the following: seen in unaffected individuals, population frequency, intact protein function, lack of segregation with disease, co-occurrence, RNA analysis, in silico models, amino acid conservation, lack of disease association in case-control studies, and/or the mechanism of disease or impacted region is inconsistent with a known cause of pathogenicity.

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

Last Updated: Nov 3, 2024