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NM_001024630.4(RUNX2):c.211C>T (p.Gln71Ter) AND Cleidocranial dysostosis

Germline classification:
Likely pathogenic (1 submission)
Last evaluated:
Nov 6, 2019
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:
RCV001253569.1

Allele description [Variation Report for NM_001024630.4(RUNX2):c.211C>T (p.Gln71Ter)]

NM_001024630.4(RUNX2):c.211C>T (p.Gln71Ter)

Genes:
RUNX2:RUNX family transcription factor 2 [Gene - OMIM - HGNC]
LOC109611589:runt related transcription factor 2 polyalanine expansion region [Gene]
Variant type:
single nucleotide variant
Cytogenetic location:
6p21.1
Genomic location:
Preferred name:
NM_001024630.4(RUNX2):c.211C>T (p.Gln71Ter)
HGVS:
  • NC_000006.12:g.45422745C>T
  • NG_008020.2:g.99429C>T
  • NG_052657.1:g.167C>T
  • NM_001015051.4:c.211C>T
  • NM_001024630.4:c.211C>TMANE SELECT
  • NM_001278478.2:c.169C>T
  • NM_001369405.1:c.169C>T
  • NP_001015051.3:p.Gln71Ter
  • NP_001019801.3:p.Gln71Ter
  • NP_001265407.1:p.Gln57Ter
  • NP_001356334.1:p.Gln57Ter
  • NC_000006.11:g.45390482C>T
  • NM_001024630.3:c.211C>T
Protein change:
Q57*
Links:
dbSNP: rs774631263
NCBI 1000 Genomes Browser:
rs774631263
Molecular consequence:
  • NM_001015051.4:c.211C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001024630.4:c.211C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001278478.2:c.169C>T - nonsense - [Sequence Ontology: SO:0001587]
  • NM_001369405.1:c.169C>T - nonsense - [Sequence Ontology: SO:0001587]
Observations:
1

Condition(s)

Name:
Cleidocranial dysostosis (CLCD1)
Synonyms:
Marie-Sainton disease; CLEIDOCRANIAL DYSPLASIA 1; Cleidocranial Dysplasia
Identifiers:
MONDO: MONDO:0007340; MedGen: C0008928; Orphanet: 1452; OMIM: 119600

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV001429357Institute of Human Genetics, University of Leipzig Medical Center
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely pathogenic
(Nov 6, 2019) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlineyes1not 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 Institute of Human Genetics, University of Leipzig Medical Center, SCV001429357.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not provided1not providednot providedclinical testing PubMed (1)
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlineyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Mar 16, 2024