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NM_183357.3(ADCY5):c.3696G>A (p.Thr1232=) AND Dyskinesia with orofacial involvement, autosomal recessive

Germline classification:
Benign (1 submission)
Last evaluated:
Dec 5, 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:
RCV002253642.1

Allele description [Variation Report for NM_183357.3(ADCY5):c.3696G>A (p.Thr1232=)]

NM_183357.3(ADCY5):c.3696G>A (p.Thr1232=)

Gene:
ADCY5:adenylate cyclase 5 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
3q21.1
Genomic location:
Preferred name:
NM_183357.3(ADCY5):c.3696G>A (p.Thr1232=)
HGVS:
  • NC_000003.12:g.123284698C>T
  • NG_033882.1:g.168848G>A
  • NM_001199642.1:c.2646G>A
  • NM_001378259.1:c.3771G>A
  • NM_183357.3:c.3696G>AMANE SELECT
  • NP_001186571.1:p.Thr882=
  • NP_001365188.1:p.Thr1257=
  • NP_899200.1:p.Thr1232=
  • NP_899200.1:p.Thr1232=
  • NC_000003.11:g.123003545C>T
  • NC_000003.11:g.123003545C>T
  • NM_183357.2:c.3696G>A
Links:
dbSNP: rs140582739
NCBI 1000 Genomes Browser:
rs140582739
Molecular consequence:
  • NM_001199642.1:c.2646G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001378259.1:c.3771G>A - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_183357.3:c.3696G>A - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Name:
Dyskinesia with orofacial involvement, autosomal recessive
Identifiers:
MONDO: MONDO:0030625; MedGen: C5562036; OMIM: 619647

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV002524624Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benign
(Dec 5, 2021) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenonot 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 Genome-Nilou Lab, SCV002524624.1

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

Last Updated: Sep 29, 2024