IthaID: 2296



Names and Sequences

Functionality: Disease modifying mutation Pathogenicity: N/A
Common Name: CD 319 (+1bp): (+G) HGVS Name: NG_013087.1:g.7184dupG

Context nucleotide sequence:
CTGCACGTGGGAAGGCTGCGGCTGG [-/G] AGATTCGCGCGCTCGGACGAGCTGA (Strand: -)

Also known as:

Comments: Protein change: Arg319GlufsX34. Cause borderline HbA2

We follow the HGVS sequence variant nomenclature and IUPAC standards.

External Links

Phenotype

Allele Phenotype (Cis):N/A
Allele Phenotype (Trans):Increased expression for δ
Associated Phenotypes: N/A

Location

Chromosome: 19
Locus: NG_013087.1
Locus Location: 7184
Size: 1 bp
Located at: KLF1
Specific Location: Exon 3

Other details

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

In silico pathogenicity prediction

Sequence Viewer

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Publications / Origin

  1. Perseu L, Satta S, Moi P, Demartis FR, Manunza L, Sollaino MC, Barella S, Cao A, Galanello R, KLF1 gene mutations cause borderline HbA(2)., Blood , 118(16), 4454-8, 2011 PubMed
Created on 2013-12-20 14:34:46, Last reviewed on 2014-03-20 11:05:01 (Show full history)

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