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NM_004082.5(DCTN1):c.*122A>C AND not provided

Germline classification:
Benign (1 submission)
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:
RCV004709944.1

Allele description [Variation Report for NM_004082.5(DCTN1):c.*122A>C]

NM_004082.5(DCTN1):c.*122A>C

Gene:
DCTN1:dynactin subunit 1 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
2p13.1
Genomic location:
Preferred name:
NM_004082.5(DCTN1):c.*122A>C
HGVS:
  • NC_000002.12:g.74361377T>G
  • NG_008735.2:g.35711A>C
  • NM_001135040.3:c.*122A>C
  • NM_001135041.3:c.*122A>C
  • NM_001190836.2:c.*122A>C
  • NM_001190837.2:c.*122A>C
  • NM_001378991.1:c.*122A>C
  • NM_001378992.1:c.*122A>C
  • NM_004082.5:c.*122A>CMANE SELECT
  • NM_023019.4:c.*122A>C
  • LRG_237t1:c.*122A>C
  • LRG_237:g.35711A>C
  • NC_000002.11:g.74588504T>G
  • NM_004082.4:c.*122A>C
  • NR_033935.2:n.4007A>C
Links:
dbSNP: rs777649011
NCBI 1000 Genomes Browser:
rs777649011
Molecular consequence:
  • NM_001135040.3:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001135041.3:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001190836.2:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001190837.2:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001378991.1:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_001378992.1:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_004082.5:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NM_023019.4:c.*122A>C - 3 prime UTR variant - [Sequence Ontology: SO:0001624]
  • NR_033935.2:n.4007A>C - non-coding transcript variant - [Sequence Ontology: SO:0001619]

Condition(s)

Synonyms:
none provided; RECLASSIFIED - ADRA2C POLYMORPHISM; RECLASSIFIED - ADRB1 POLYMORPHISM
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV005242986Breakthrough Genomics, Breakthrough Genomics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benigngermlinenot provided

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyesnot providednot providednot providednot providednot providednot provided

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 Breakthrough Genomics, Breakthrough Genomics, SCV005242986.1

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

Last Updated: Jan 13, 2025