Original source

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

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

Chromosome X:154153068 (forward strand) | View in location tab


with COSMIC COSM3759420 (T/G), COSM3759419 (T/G) ; HGMD-PUBLIC CM045803

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 35 sample genotypes and is associated with 2 phenotypes.

Variant displays