NM_018451.5(CPAP):c.3704-14_3704-12del AND Seckel syndrome 4

Germline classification:: Benign (1 submission)
Last evaluated:: Jul 22, 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:: RCV001578979.3

Allele description [Variation Report for NM_018451.5(CPAP):c.3704-14_3704-12del]

NM_018451.5(CPAP):c.3704-14_3704-12del

Genes:

CPAP:centrosome assembly and centriole elongation protein [Gene - OMIM - HGNC]
RNF17:ring finger protein 17 [Gene - OMIM - HGNC]

Variant type:

Microsatellite

Cytogenetic location:

13q12.12

Genomic location:

Preferred name:

NM_018451.5(CPAP):c.3704-14_3704-12del

HGVS:

NC_000013.11:g.24884095GTT[1]
NG_009165.2:g.43848AAC[1]
NM_018451.5:c.3704-14_3704-12delMANE SELECT
NC_000013.10:g.25458233GTT[1]
NC_000013.10:g.25458233_25458235del
NM_018451.3:c.3704-14_3704-12del
NM_018451.3:c.3704-14_3704-12delAAC
NM_018451.4:c.3704-14_3704-12delAAC

Links:

dbSNP: rs34991318

NCBI 1000 Genomes Browser:

rs34991318

Molecular consequence:

NM_018451.5:c.3704-14_3704-12del - intron variant - [Sequence Ontology: SO:0001627]

Condition(s)

Name:: Seckel syndrome 4 (SCKL4)
Identifiers:: MONDO: MONDO:0013358; MedGen: C3888212; Orphanet: 808; OMIM: 613676

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001806357	Genome-Nilou Lab	criteria provided, single submitter (ACMG Guidelines, 2015)	Benign (Jul 22, 2021)	germline	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

SCV001806357

Genome-Nilou Lab

criteria provided, single submitter

(ACMG Guidelines, 2015)

Benign
(Jul 22, 2021)

germline

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	germline	no	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 Genome-Nilou Lab, SCV001806357.1

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

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	no	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Feb 25, 2025

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