Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

T/A|Ambiguity code: W

Chromosome Y:2787224 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM941304, CM021699

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB 2010_April_001_019_SRY_480000_0023, 8628

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays