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NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=) AND not specified

Germline classification:
Likely benign (1 submission)
Last evaluated:
Dec 29, 2017
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:
RCV001821108.4

Allele description [Variation Report for NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=)]

NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=)

Gene:
CDK5RAP2:CDK5 regulatory subunit associated protein 2 [Gene - OMIM - HGNC]
Variant type:
single nucleotide variant
Cytogenetic location:
9q33.2
Genomic location:
Preferred name:
NM_018249.6(CDK5RAP2):c.5649A>G (p.Pro1883=)
HGVS:
  • NC_000009.12:g.120389269T>C
  • NG_008999.1:g.195891A>G
  • NM_001011649.3:c.5412A>G
  • NM_001272039.2:c.4959A>G
  • NM_018249.6:c.5649A>GMANE SELECT
  • NP_001011649.1:p.Pro1804=
  • NP_001258968.1:p.Pro1653=
  • NP_060719.4:p.Pro1883=
  • NC_000009.11:g.123151547T>C
  • NM_018249.5:c.5649A>G
  • NR_073554.2:n.5913A>G
  • NR_073555.2:n.5836A>G
  • NR_073556.2:n.6045A>G
  • NR_073557.2:n.5918A>G
  • NR_073558.2:n.5915A>G
Links:
dbSNP: rs199736016
NCBI 1000 Genomes Browser:
rs199736016
Molecular consequence:
  • NR_073554.2:n.5913A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_073555.2:n.5836A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_073556.2:n.6045A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_073557.2:n.5918A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NR_073558.2:n.5915A>G - non-coding transcript variant - [Sequence Ontology: SO:0001619]
  • NM_001011649.3:c.5412A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_001272039.2:c.4959A>G - synonymous variant - [Sequence Ontology: SO:0001819]
  • NM_018249.6:c.5649A>G - synonymous variant - [Sequence Ontology: SO:0001819]

Condition(s)

Synonyms:
AllHighlyPenetrant
Identifiers:
MedGen: CN169374

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV002068267Genetic Services Laboratory, University of Chicago
criteria provided, single submitter

(ACMG Guidelines, 2015)
Likely benign
(Dec 29, 2017)
germlineclinical testing

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

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 Genetic Services Laboratory, University of Chicago, SCV002068267.1

#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: Oct 8, 2024