Variants
Sign InSign Up

rs754254864

  • Uncertain significance

Your Genotype

Sign In

Description

This sequence change replaces arginine, which is basic and polar, with tryptophan, which is neutral and slightly polar, at codon 732 of the SULF1 protein (p.Arg732Trp). This variant is present in population databases (rs754254864, gnomAD 0.02%). This variant has not been reported in the literature in individuals affected with SULF1-related conditions. ClinVar contains an entry for this variant (Variation ID: 282083). Algorithms developed to predict the effect of missense changes on protein structure and function are either unavailable or do not agree on the potential impact of this missense change (SIFT: "Deleterious"; PolyPhen-2: "Probably Damaging"; Align-GVGD: "Class C0"). 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

A

T

Chromosome

8


Location

69629589


Variant Type

SNP

Genes

ClinVar

Name

NM_001128205.2(SULF1):c.2194C>T (p.Arg732Trp)


Allele

T


Clinical Significance

Uncertain significance

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.