Original source

Variants (including SNPs and indels) imported from dbSNP (release 139) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Z:1604907 (forward strand) | View in location tab

Most severe consequence
 
Missense variant

This variant has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays