NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile) AND Neuroblastoma

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Apr 27, 2017
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:: RCV001098679.12

Allele description [Variation Report for NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile)]

NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile)

Gene:

KIF1B:kinesin family member 1B [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

1p36.22

Genomic location:

Preferred name:

NM_001365951.3(KIF1B):c.2618C>T (p.Thr873Ile)

HGVS:

NC_000001.11:g.10324838C>T
NG_008069.1:g.119133C>T
NM_001365951.3:c.2618C>TMANE SELECT
NM_001365952.1:c.2618C>T
NM_015074.3:c.2480C>T
NP_001352880.1:p.Thr873Ile
NP_001352881.1:p.Thr873Ile
NP_055889.2:p.Thr827Ile
LRG_252t1:c.2480C>T
LRG_252t2:c.2618C>T
LRG_252:g.119133C>T
LRG_252p1:p.Thr827Ile
LRG_252p2:p.Thr873Ile
NC_000001.10:g.10384896C>T

Protein change:

T827I; THR827ILE

Links:

OMIM: 605995.0003; dbSNP: rs121908162

NCBI 1000 Genomes Browser:

rs121908162

Molecular consequence:

NM_001365951.3:c.2618C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_001365952.1:c.2618C>T - missense variant - [Sequence Ontology: SO:0001583]
NM_015074.3:c.2480C>T - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Neuroblastoma (NB)
Identifiers:: MONDO: MONDO:0005072; MeSH: D009447; MedGen: C0027819; Orphanet: 635; Human Phenotype Ontology: HP:0003006

Recent activity

Clear Turn Off Turn On

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

Help

Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV001255062	Illumina Laboratory Services, Illumina	criteria provided, single submitter (ICSL Variant Classification Criteria 13 December 2019)	Uncertain significance (Apr 27, 2017)	germline	clinical testing	PubMed (2) [See all records that cite these PMIDs] 24469107, 18334619 Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV001255062

Illumina Laboratory Services, Illumina

criteria provided, single submitter

(ICSL Variant Classification Criteria 13 December 2019)

Uncertain significance
(Apr 27, 2017)

germline

clinical testing

PubMed (2)
[See all records that cite these PMIDs]

Citation Link

Help

Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Citations

PubMed

RNA helicase A is a downstream mediator of KIF1Bβ tumor-suppressor function in neuroblastoma.

Chen ZX, Wallis K, Fell SM, Sobrado VR, Hemmer MC, Ramsköld D, Hellman U, Sandberg R, Kenchappa RS, Martinson T, Johnsen JI, Kogner P, Schlisio S.

Cancer Discov. 2014 Apr;4(4):434-51. doi: 10.1158/2159-8290.CD-13-0362. Epub 2014 Jan 27.

PubMed [citation]

PMID:: 24469107

The kinesin KIF1Bbeta acts downstream from EglN3 to induce apoptosis and is a potential 1p36 tumor suppressor.

Schlisio S, Kenchappa RS, Vredeveld LC, George RE, Stewart R, Greulich H, Shahriari K, Nguyen NV, Pigny P, Dahia PL, Pomeroy SL, Maris JM, Look AT, Meyerson M, Peeper DS, Carter BD, Kaelin WG Jr.

Genes Dev. 2008 Apr 1;22(7):884-93. doi: 10.1101/gad.1648608. Epub 2008 Mar 11.

PubMed [citation]

PMID:: 18334619
PMCID:: PMC2279200

Details of each submission

From Illumina Laboratory Services, Illumina, SCV001255062.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	PubMed (2)

Description

This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). Publications were found based on this search. However, the evidence from the literature, in combination with allele frequency data from public databases where available, was not sufficient to rule this variant in or out of causing disease. Therefore, this variant is classified as a variant of unknown significance.

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

Last Updated: Nov 3, 2024

ClinVar

Relating variation to medicine