IthaID: 3667


Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs757369 HGVS Name: NC_000014.9:g.68506829A>G

Context nucleotide sequence:
TTTTGTGCTTGGGTATGTGTGCAC [A>G] CATGGTAGGCGCCCACACTCAAGT (Strand: +)

Also known as:

Comments: Associated with F-cell levels in a pediatric cohort with sickle cell anaemia from the Silent Cerebral Infarct Transfusion (SIT) trial.

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: F-cell numbers

Location

Chromosome: 14
Locus: NG_023267.2
Locus Location: 692051
Size: 1 bp
Located at: RAD51B
Specific Location: Intron 10

Other details

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

In silico pathogenicity prediction

Publications / Origin

  1. Bhatnagar P, Purvis S, Barron-Casella E, DeBaun MR, Casella JF, Arking DE, Keefer JR, Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients., J. Hum. Genet. , 56(4), 316-23, 2011
Created on 2020-10-15 15:46:19, Last reviewed on (Show full history)

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