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NM_001130987.2(DYSF):c.3190C>T (p.Arg1064Cys) AND not provided

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Mar 4, 2023
Review status:
2 stars out of maximum of 4 stars
criteria provided, multiple submitters, no conflicts
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:
RCV003144306.3

Allele description [Variation Report for NM_001130987.2(DYSF):c.3190C>T (p.Arg1064Cys)]

NM_001130987.2(DYSF):c.3190C>T (p.Arg1064Cys)

Gene:
DYSF:dysferlin [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2p13.2
Genomic location:
Preferred name:
NM_001130987.2(DYSF):c.3190C>T (p.Arg1064Cys)
HGVS:
  • NC_000002.12:g.71570703C>T
  • NG_008694.1:g.122081C>T
  • NM_001130455.2:c.3139C>T
  • NM_001130976.2:c.3094C>T
  • NM_001130977.2:c.3094C>T
  • NM_001130978.2:c.3136C>T
  • NM_001130979.2:c.3229C>T
  • NM_001130980.2:c.3187C>T
  • NM_001130981.2:c.3187C>T
  • NM_001130982.2:c.3232C>T
  • NM_001130983.2:c.3139C>T
  • NM_001130984.2:c.3097C>T
  • NM_001130985.2:c.3190C>T
  • NM_001130986.2:c.3097C>T
  • NM_001130987.2:c.3190C>TMANE SELECT
  • NM_003494.4:c.3136C>T
  • NP_001123927.1:p.Arg1047Cys
  • NP_001124448.1:p.Arg1032Cys
  • NP_001124449.1:p.Arg1032Cys
  • NP_001124450.1:p.Arg1046Cys
  • NP_001124451.1:p.Arg1077Cys
  • NP_001124452.1:p.Arg1063Cys
  • NP_001124453.1:p.Arg1063Cys
  • NP_001124454.1:p.Arg1078Cys
  • NP_001124455.1:p.Arg1047Cys
  • NP_001124456.1:p.Arg1033Cys
  • NP_001124457.1:p.Arg1064Cys
  • NP_001124458.1:p.Arg1033Cys
  • NP_001124459.1:p.Arg1064Cys
  • NP_003485.1:p.Arg1046Cys
  • LRG_845t1:c.3136C>T
  • LRG_845t2:c.3190C>T
  • LRG_845:g.122081C>T
  • LRG_845p1:p.Arg1046Cys
  • LRG_845p2:p.Arg1064Cys
  • NC_000002.11:g.71797833C>T
  • NM_003494.3:c.3136C>T
Protein change:
R1032C
Links:
dbSNP: rs752810646
NCBI 1000 Genomes Browser:
rs752810646
Molecular consequence:
  • NM_001130455.2:c.3139C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130976.2:c.3094C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130977.2:c.3094C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130978.2:c.3136C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130979.2:c.3229C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130980.2:c.3187C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130981.2:c.3187C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130982.2:c.3232C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130983.2:c.3139C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130984.2:c.3097C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130985.2:c.3190C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130986.2:c.3097C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001130987.2:c.3190C>T - missense variant - [Sequence Ontology: SO:0001583]
  • NM_003494.4:c.3136C>T - missense variant - [Sequence Ontology: SO:0001583]

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
SCV003831284Revvity Omics, Revvity
criteria provided, single submitter

(ACMG Guidelines, 2015)		Uncertain significance
(Jul 12, 2019) 		germlineclinical testing

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

SCV003837186GeneDx
criteria provided, single submitter

(GeneDx Variant Classification Process June 2021)		Uncertain significance
(Mar 4, 2023) 		germlineclinical testing

Citation Link

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providedclinical testing
not providedgermlineunknownnot 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 Revvity Omics, Revvity, SCV003831284.2

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

From GeneDx, SCV003837186.1

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

Description

In silico analysis supports that this missense variant has a deleterious effect on protein structure/function; Has not been previously published as pathogenic or benign to our knowledge; This variant is associated with the following publications: (PMID: 24438169)

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

Last Updated: Sep 29, 2024