NM_015634.4(KIFBP):c.169G>T (p.Glu57Ter) AND Goldberg-Shprintzen syndrome

Germline classification:: Likely pathogenic (1 submission)
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:: RCV001251036.1

Allele description [Variation Report for NM_015634.4(KIFBP):c.169G>T (p.Glu57Ter)]

NM_015634.4(KIFBP):c.169G>T (p.Glu57Ter)

Gene:

KIFBP:kinesin family binding protein [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

10q22.1

Genomic location:

Preferred name:

NM_015634.4(KIFBP):c.169G>T (p.Glu57Ter)

HGVS:

NC_000010.11:g.68989001G>T
NG_017061.1:g.5281G>T
NM_015634.4:c.169G>TMANE SELECT
NP_056449.1:p.Glu57Ter
NC_000010.10:g.70748757G>T
NM_015634.3:c.169G>T

Protein change:

E57*

Links:

dbSNP: rs770201721

NCBI 1000 Genomes Browser:

rs770201721

Molecular consequence:

NM_015634.4:c.169G>T - nonsense - [Sequence Ontology: SO:0001587]

Condition(s)

Name:: Goldberg-Shprintzen syndrome
Identifiers:: MONDO: MONDO:0012280; MedGen: C1836123; Orphanet: 66629; OMIM: 609460

Recent activity

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IKK interacting protein [Homo sapiens]
IKK interacting protein [Homo sapiens]
gi|127797393|gb|AAH29415.2|

Protein
Tulasnella sp. AP-79c internal transcribed spacer 1, partial sequence; 5.8S ribo...
Tulasnella sp. AP-79c internal transcribed spacer 1, partial sequence; 5.8S ribosomal RNA gene, complete sequence; and internal transcribed spacer 2, partial sequence
gi|112430806|gb|DQ834399.1|

Nucleotide
Homo sapiens complement C1q B chain (C1QB), RefSeqGene (LRG_23) on chromosome 1
Homo sapiens complement C1q B chain (C1QB), RefSeqGene (LRG_23) on chromosome 1
gi|163965408|ref|NG_007283.1||gnl|L G_23

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001426432	Centogene AG - the Rare Disease Company	criteria provided, single submitter (ACMG Guidelines, 2015)	Likely pathogenic	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

SCV001426432

Centogene AG - the Rare Disease Company

criteria provided, single submitter

(ACMG Guidelines, 2015)

Likely pathogenic

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	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 Centogene AG - the Rare Disease Company, SCV001426432.1

#	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	yes	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Sep 16, 2024

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