NM_001260.3(CDK8):c.212G>A (p.Arg71Gln) AND Intellectual developmental disorder with hypotonia and behavioral abnormalities

Germline classification:: Likely benign (1 submission)
Last evaluated:: Nov 19, 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:: RCV002287232.1

Allele description [Variation Report for NM_001260.3(CDK8):c.212G>A (p.Arg71Gln)]

NM_001260.3(CDK8):c.212G>A (p.Arg71Gln)

Gene:

CDK8:cyclin dependent kinase 8 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

13q12.13

Genomic location:

Preferred name:

NM_001260.3(CDK8):c.212G>A (p.Arg71Gln)

HGVS:

NC_000013.11:g.26349079G>A
NM_001260.3:c.212G>AMANE SELECT
NM_001318368.2:c.212G>A
NM_001346501.2:c.-250G>A
NP_001251.1:p.Arg71Gln
NP_001305297.1:p.Arg71Gln
NC_000013.10:g.26923216G>A

Protein change:

R71Q

Molecular consequence:

NM_001346501.2:c.-250G>A - 5 prime UTR variant - [Sequence Ontology: SO:0001623]
NM_001260.3:c.212G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001318368.2:c.212G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Intellectual developmental disorder with hypotonia and behavioral abnormalities
Identifiers:: MONDO: MONDO:0032897; MedGen: C5231489; OMIM: 618748

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002577462	Laboratory of Medical Genetics, National & Kapodistrian University of Athens	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely benign (Nov 19, 2021)	paternal	clinical testing	PubMed (1) [See all records that cite this PMID]

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV002577462

Laboratory of Medical Genetics, National & Kapodistrian University of Athens

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely benign
(Nov 19, 2021)

paternal

clinical testing

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

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	paternal	yes	not provided	not provided	not provided	not provided	not provided	clinical 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 Laboratory of Medical Genetics, National & Kapodistrian University of Athens, SCV002577462.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (1)

Description

PM2, PP2, PP3, BS2

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	paternal	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Oct 8, 2022

ClinVar

Relating variation to medicine