Original source

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

Alleles
A/T | Ambiguity code: W
Location

Chromosome Y:2787592 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM971421, CD991879

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_014_SRY_480000_0018, 8623

This variation has 5 HGVS names - click the plus to show

Y:g.2787592A>T
ENST00000623823.1:c.12T>A
ENSP00000485519.1:p.Tyr4Ter
ENST00000383070.1:c.12T>A
ENSP00000372547.1:p.Tyr4Ter

Variation displays