Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome X:43731838 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_014795

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2 sample genotypes and is mentioned in 4 citations.

Variant displays