Original source

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

Alleles
G/A|Ambiguity code: R
Location

Chromosome Y:2787207 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM971423, CM068437

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 8624, 2010_April_001_015_SRY_480000_0019

HGVS names

This variant has 3 HGVS names - Hide

Y:g.2787207G>A
ENST00000383070.1:c.397C>T
ENSP00000372547.1:p.Arg133Trp

About this variant

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

Variant displays