NM_001365951.3(KIF1B):c.3434G>A (p.Arg1145His) AND multiple conditions

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Dec 23, 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:: RCV002504522.1

Allele description [Variation Report for NM_001365951.3(KIF1B):c.3434G>A (p.Arg1145His)]

NM_001365951.3(KIF1B):c.3434G>A (p.Arg1145His)

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.3434G>A (p.Arg1145His)

HGVS:

NC_000001.11:g.10339780G>A
NG_008069.1:g.134075G>A
NM_001365951.3:c.3434G>AMANE SELECT
NM_001365952.1:c.3434G>A
NM_015074.3:c.3296G>A
NP_001352880.1:p.Arg1145His
NP_001352881.1:p.Arg1145His
NP_055889.2:p.Arg1099His
LRG_252t1:c.3296G>A
LRG_252t2:c.3434G>A
LRG_252:g.134075G>A
LRG_252p1:p.Arg1099His
LRG_252p2:p.Arg1145His
NC_000001.10:g.10399838G>A

Protein change:

R1099H

Links:

dbSNP: rs373663596

NCBI 1000 Genomes Browser:

rs373663596

Molecular consequence:

NM_001365951.3:c.3434G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_001365952.1:c.3434G>A - missense variant - [Sequence Ontology: SO:0001583]
NM_015074.3:c.3296G>A - missense variant - [Sequence Ontology: SO:0001583]

Condition(s)

Name:: Charcot-Marie-Tooth disease type 2A1
Synonyms:: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2A1; CHARCOT-MARIE-TOOTH DISEASE, AXONAL, AUTOSOMAL DOMINANT, TYPE 2A1; CHARCOT-MARIE-TOOTH DISEASE, NEURONAL, TYPE 2A1; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0007308; MedGen: C1861678; Orphanet: 99946; OMIM: 118210

Name:: Pheochromocytoma
Synonyms:: Chromaffinoma; Chromaffin paraganglioma; Chromaffin tumor; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0008233; MedGen: C0031511; Orphanet: 29072; OMIM: 171300; Human Phenotype Ontology: HP:0002666

Name:: Neuroblastoma, susceptibility to, 1
Synonyms:: Neuroblastoma 1
Identifiers:: MONDO: MONDO:0009741; MedGen: C2749485; OMIM: 256700

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV002816168	Fulgent Genetics, Fulgent Genetics	criteria provided, single submitter (ACMG Guidelines, 2015)	Uncertain significance (Dec 23, 2021)	unknown	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

SCV002816168

Fulgent Genetics, Fulgent Genetics

criteria provided, single submitter

(ACMG Guidelines, 2015)

Uncertain significance
(Dec 23, 2021)

unknown

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	unknown	unknown	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 Fulgent Genetics, Fulgent Genetics, SCV002816168.1

#	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	unknown	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: Nov 24, 2024

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