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NM_004006.3(DMD):c.3029C>T (p.Ala1010Val) AND multiple conditions

Germline classification:
Uncertain significance (1 submission)
Last evaluated:
Aug 17, 2021
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:
RCV002493789.1

Allele description [Variation Report for NM_004006.3(DMD):c.3029C>T (p.Ala1010Val)]

NM_004006.3(DMD):c.3029C>T (p.Ala1010Val)

Gene:
DMD:dystrophin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
Xp21.1
Genomic location:
Preferred name:
NM_004006.3(DMD):c.3029C>T (p.Ala1010Val)
HGVS:
  • NC_000023.11:g.32468631G>A
  • NG_012232.1:g.875979C>T
  • NM_000109.4:c.3005C>T
  • NM_004006.3:c.3029C>TMANE SELECT
  • NM_004009.3:c.3017C>T
  • NM_004010.3:c.2660C>T
  • NP_000100.3:p.Ala1002Val
  • NP_003997.2:p.Ala1010Val
  • NP_004000.1:p.Ala1006Val
  • NP_004001.1:p.Ala887Val
  • LRG_199:g.875979C>T
  • NC_000023.10:g.32486748G>A
  • NM_004006.2:c.3029C>T
Protein change:
A1002V
Links:
dbSNP: rs780896933
NCBI 1000 Genomes Browser:
rs780896933
Molecular consequence:
  • NM_000109.4:c.3005C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004006.3:c.3029C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004009.3:c.3017C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_004010.3:c.2660C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:
Becker muscular dystrophy (BMD)
Synonyms:
Benign pseudohypertrophic muscular dystrophy; Becker's muscular dystrophy; Muscular dystrophy pseudohypertrophic progressive, Becker type
Identifiers:
MONDO: MONDO:0010311; MedGen: C0917713; Orphanet: 98895; OMIM: 300376
Name:
Duchenne muscular dystrophy (DMD)
Synonyms:
Muscular dystrophy, pseudohypertrophic progressive, Duchenne type
Identifiers:
MONDO: MONDO:0010679; MedGen: C0013264; Orphanet: 98896; OMIM: 310200
Name:
Dilated cardiomyopathy 3B (CMD3B)
Synonyms:
CARDIOMYOPATHY, DILATED, X-LINKED; CMD3B: DMD-Related Dilated Cardiomyopathy
Identifiers:
MONDO: MONDO:0010542; MedGen: C3668940; Orphanet: 154; OMIM: 302045

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002784251Fulgent Genetics, Fulgent Genetics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Aug 17, 2021) 		unknownclinical testing

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

Help

Summary from all submissions

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

Citations

PubMed

Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.

Richards S, Aziz N, Bale S, Bick D, Das S, Gastier-Foster J, Grody WW, Hegde M, Lyon E, Spector E, Voelkerding K, Rehm HL; ACMG Laboratory Quality Assurance Committee..

Genet Med. 2015 May;17(5):405-24. doi: 10.1038/gim.2015.30. Epub 2015 Mar 5.

PubMed [citation]
PMID:
25741868
PMCID:
PMC4544753

Details of each submission

From Fulgent Genetics, Fulgent Genetics, SCV002784251.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providednot providednot providednot providednot providednot providednot provided

Last Updated: Sep 29, 2024