Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

A/C | Ancestral: A | Ambiguity code: M | MAF: < 0.01 (C)

Chromosome X:19359015 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_050436

HGVS names

This variant has 13 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 13 transcripts and has 2897 sample genotypes.

Variant displays