Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
T/A | Ambiguity code: W
Location

Chromosome Y:2787224 (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 5 HGVS names - click the plus to show

Y:g.2787224T>A
ENST00000623823.1:c.380A>T
ENSP00000485519.1:p.Tyr127Phe
ENST00000383070.1:c.380A>T
ENSP00000372547.1:p.Tyr127Phe

Variation displays