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NM_001367561.1(DOCK7):c.1283-14del AND not provided

Germline classification:
Likely benign (1 submission)
Last evaluated:
Feb 2, 2016
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:
RCV000224920.2

Allele description [Variation Report for NM_001367561.1(DOCK7):c.1283-14del]

NM_001367561.1(DOCK7):c.1283-14del

Gene:
DOCK7:dedicator of cytokinesis 7 [Gene - OMIM - HGNC]
Variant type:
Deletion
Cytogenetic location:
1p31.3
Genomic location:
Preferred name:
NM_001367561.1(DOCK7):c.1283-14del
HGVS:
  • NC_000001.11:g.62625424del
  • NG_033073.2:g.67954del
  • NM_001271999.2:c.1283-14del
  • NM_001272000.2:c.1283-14del
  • NM_001272001.2:c.1283-14del
  • NM_001272002.2:c.1283-14del
  • NM_001330614.2:c.1283-14del
  • NM_001367561.1:c.1283-14delMANE SELECT
  • NM_033407.4:c.1283-14del
  • NC_000001.10:g.63091086del
  • NC_000001.10:g.63091095del
Links:
dbSNP: rs541344421
NCBI 1000 Genomes Browser:
rs541344421
Molecular consequence:
  • NM_001271999.2:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001272000.2:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001272001.2:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001272002.2:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001330614.2:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001367561.1:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]
  • NM_033407.4:c.1283-14del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Help
Submission AccessionSubmitterReview Status
(Assertion method)		Clinical Significance
(Last evaluated)		OriginMethodCitations
SCV000281638Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics
criteria provided, single submitter

(ACMG Guidelines, 2015)		Likely Benign
(Feb 2, 2016) 		germlineclinical testing

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

Help

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot providednot 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 Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics, SCV000281638.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testing PubMed (1)

Description

Converted during submission to Likely benign.

#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot providednot providednot providednot providednot provided0.007792not providednot provided

Last Updated: Sep 29, 2024