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NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del) AND not specified

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Oct 4, 2013
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:
RCV000035945.6

Allele description [Variation Report for NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del)]

NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del)

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:
Deletion
Cytogenetic location:
14q11.2
Genomic location:
Preferred name:
NM_000257.4(MYH7):c.5015_5020del (p.Ala1672_Ile1673del)
HGVS:
  • NC_000014.9:g.23415771_23415776del
  • NG_007884.1:g.24891_24896del
  • NM_000257.4:c.5015_5020delMANE SELECT
  • NP_000248.2:p.Ala1672_Ile1673del
  • LRG_384t1:c.5015_5020del
  • LRG_384:g.24891_24896del
  • NC_000014.8:g.23884975_23884980delCGATGG
  • NC_000014.8:g.23884980_23884985del
  • NM_000257.2:c.5015_5020delCCATCG
  • NR_126491.1:n.203_208del
  • c.5015_5020delCCATCG
Links:
dbSNP: rs397516234
NCBI 1000 Genomes Browser:
rs397516234
Molecular consequence:
  • NM_000257.4:c.5015_5020del - inframe_deletion - [Sequence Ontology: SO:0001822]
  • NR_126491.1:n.203_208del - non-coding transcript variant - [Sequence Ontology: SO:0001619]
Observations:
1

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000059596Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine
criteria provided, single submitter

(LMM Criteria)		Uncertain significance
(Oct 4, 2013) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided11not 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, SCV000059596.5

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)

Description

proposed classification - variant undergoing re-assessment, contact laboratory

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot provided1not provided1not provided

Last Updated: Mar 26, 2023