IthaID: 3116


Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs1799963 HGVS Name: NG_008953.1:g.25313G>A

Context nucleotide sequence:
GTTCCCAATAAAAGTGACTCTCAGY [A/G] AGCCTCAATGCTCCCAGTGCTATTC (Strand: +)

Also known as:

Comments: This SNP was described in a splenectomized patient with HbH disease and recurrent thromboembolism. It presents a significant risk factor for venous thrombosis.

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

Phenotype

Allele Phenotype (Cis):N/A
Allele Phenotype (Trans):N/A
Associated Phenotypes: Thromboembolism [HP:0001907]

Location

Chromosome: 11
Locus: NG_008953.1
Locus Location: 25313
Size: 1 bp
Located at: F2
Specific Location: 3'UTR

Other details

Type of Mutation: Point-Mutation(Substitution)
Effect on Gene/Protein Function: N/A
Ethnic Origin: Chinese Han
Molecular mechanism: N/A
Inheritance: Quantitative trait
DNA Sequence Determined: Yes

In silico pathogenicity prediction

Publications / Origin

  1. Sun NA, Cheng P, Deng DH, Liu RR, Lai YR, Analysis of the genetic variants associated with recurrent thromboembolism in a patient with hemoglobin H disease following splenectomy: A case report., Biomed Rep , 5(1), 23-26, 2016
Created on 2016-09-29 18:21:31, Last reviewed on (Show full history)

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