IthaID: 3511



Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs7507634 HGVS Name: NC_000019.10:g.10325886C>T

Context nucleotide sequence:
CTGATCATGAAGCACTGCCAGCCC [C>T] ATTTTGAGATGTGGAAACAGGCTA (Strand: +)

Also known as:

Comments: SNP associated with episodes of pain in patients from the Cooperative Study of Sickle Cell Disease (CSSCD, n=1514). The association was not replicated in a second, independent group of patients from the CSSCD (n=387).

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: Pain [HP:0012531]

Location

Chromosome: 19
Locus: NM_133452.3
Locus Location: N/A
Size: 1 bp
Located at: RAVER1
Specific Location: Intron 3

Other details

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

In silico pathogenicity prediction

Sequence Viewer

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Publications / Origin

  1. Galarneau G, Coady S, Garrett ME, Jeffries N, Puggal M, Paltoo D, Soldano K, Guasch A, Ashley-Koch AE, Telen MJ, Kutlar A, Lettre G, Papanicolaou GJ, Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients., Blood , 122(3), 434-42, 2013 PubMed
Created on 2019-11-29 12:11:47, Last reviewed on (Show full history)

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