Original source

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

T/A | Ancestral: T | Ambiguity code: W

Chromosome X:120456678 (forward strand) | View in location tab


with COSMIC COSM4156559 (T/A), COSM4156558 (T/A), COSM4156557 (T/A)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 1484 sample genotypes and is associated with 2 phenotypes.

Variant displays