Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome X:154765480 (forward strand) | View in location tab


with COSMIC COSM1557490 (G/T) ; HGMD-PUBLIC CM990476

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays