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NM_006721.4(ADK):c.878-71T>C AND Adenosine kinase deficiency

Germline classification:
Benign (1 submission)
Last evaluated:
Jul 14, 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:
RCV001549249.2

Allele description [Variation Report for NM_006721.4(ADK):c.878-71T>C]

NM_006721.4(ADK):c.878-71T>C

Gene:
ADK:adenosine kinase [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
10q22.2
Genomic location:
Preferred name:
NM_006721.4(ADK):c.878-71T>C
HGVS:
  • NC_000010.11:g.74670112T>C
  • NG_030484.2:g.523928T>C
  • NM_001123.4:c.827-71T>C
  • NM_001202449.2:c.773-71T>C
  • NM_001202450.2:c.707-71T>C
  • NM_001369123.1:c.763-71T>C
  • NM_001369124.1:c.656-71T>C
  • NM_006721.4:c.878-71T>CMANE SELECT
  • NC_000010.10:g.76429870T>C
Links:
dbSNP: rs10740443
NCBI 1000 Genomes Browser:
rs10740443
Molecular consequence:
  • NM_001123.4:c.827-71T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001202449.2:c.773-71T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001202450.2:c.707-71T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369123.1:c.763-71T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001369124.1:c.656-71T>C - intron variant - [Sequence Ontology: SO:0001627]
  • NM_006721.4:c.878-71T>C - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:
Adenosine kinase deficiency
Synonyms:
Hypermethioninemia due to adenosine kinase deficiency; MENTAL RETARDATION, AUTOSOMAL RECESSIVE 8
Identifiers:
MONDO: MONDO:0100255; MedGen: C4706555; Orphanet: 289290; Orphanet: 88616; OMIM: 614300

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001769369Genome-Nilou Lab
criteria provided, single submitter

(ACMG Guidelines, 2015)		Benign
(Jul 14, 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, SCV001769369.1

#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