Original source

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

C/A/T | Ancestral: C | Ambiguity code: H

Chromosome X:37796131 (forward strand) | View in location tab


with HGMD-PUBLIC CM980470, CM980471 ; PhenCode CYBBbase_D0025:g.17064C>T (C/T), CYBBbase_D0025:g.17064C>A (C/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, is associated with 3 phenotypes and is mentioned in 1 citation.

Variant displays