Variants
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rs1567728589

  • Uncertain significance

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Description

This sequence change replaces arginine with threonine at codon 1085 of the BRIP1 protein (p.Arg1085Thr). The arginine residue is weakly conserved and there is a moderate physicochemical difference between arginine and threonine. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals affected with BRIP1-related conditions. Algorithms developed to predict the effect of missense changes on protein structure and function (SIFT, PolyPhen-2, Align-GVGD) all suggest that this variant is likely to be tolerated. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.

Reference Allele

C


Alternative Allele

G

Chromosome

17


Location

61683792


Variant Type

SNP

Genes

ClinVar

Name

NM_032043.3(BRIP1):c.3254G>C (p.Arg1085Thr)


Allele

G


Clinical Significance

Uncertain significance

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