Original source

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

Alleles
T/C | Ambiguity code: Y
Location

Chromosome Y:12702062 (forward strand) | View in location tab

Most severe consequence
 
Splice region variant
Evidence status

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

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature and has 1 sample genotype.

Variant displays