IthaID: 2735



Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs1008140 HGVS Name: NG_011992.1:g.22464T>C

Context nucleotide sequence:
ggaaagctaagggctttacataaag [C/T] atctcatttaatcttcaccagaaca (Strand: +)

Also known as:

Comments: SNP associated with HbF levels in the younger subjects (<24 years; n=980) of the Cooperative Study of Sickle Cell Disease (CSSCD).

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: Hb F levels [HP:0011904] [OMIM:141749]

Location

Chromosome: 7
Locus: NG_011992.1
Locus Location: 22464
Size: 1 bp
Located at: NOS3
Specific Location: Intron 17

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. Sebastiani P, Wang L, Nolan VG, Melista E, Ma Q, Baldwin CT, Steinberg MH, Fetal hemoglobin in sickle cell anemia: Bayesian modeling of genetic associations., Am. J. Hematol. , 83(3), 189-95, 2008 PubMed
Created on 2016-05-13 15:14:13, Last reviewed on (Show full history)

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