IthaID: 2644



Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: rs2157256 HGVS Name: NG_011884.2:g.81403T>C

Context nucleotide sequence:
GGCCTCAAGAGCTTGTTTAATCCAC [A/G] TAATCCTGTATGGTGGGTGGTCATT (Strand: +)

Also known as:

Comments: SNP associated with focal segmental glomerulosclerosis in African Americans (56 cases; 1759 controls).

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: Focal segmental glomerulosclerosis [HP:0000097]

Location

Chromosome: 22
Locus: NG_011884.2
Locus Location: 81403
Size: 1 bp
Located at: MYH9
Specific Location: Intron 14

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. Genovese G, Tonna SJ, Knob AU, Appel GB, Katz A, Bernhardy AJ, Needham AW, Lazarus R, Pollak MR, A risk allele for focal segmental glomerulosclerosis in African Americans is located within a region containing APOL1 and MYH9., Kidney Int. , 78(7), 698-704, 2010 PubMed
Created on 2016-05-10 16:33:18, Last reviewed on (Show full history)

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