Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ambiguity code: W
Location

Chromosome Y:2655265 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021699, CM941304

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_019_SRY_480000_0023, 8628

This variation has 7 HGVS names - click the plus to show

Y:g.2655265T>A
ENST00000534739.2:c.380A>T
ENSP00000438917.1:p.Tyr127Phe
ENST00000525526.2:c.380A>T
ENSP00000437575.1:p.Tyr127Phe
ENST00000383070.1:c.380A>T
ENSP00000372547.1:p.Tyr127Phe

Variation displays