Original source

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

Alleles
A/T | Ambiguity code: W
Location

Chromosome Y:2655633 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD991879, CM971421

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_014_SRY_480000_0018, 8623

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

Y:g.2655633A>T
ENST00000534739.2:c.12T>A
ENSP00000438917.1:p.Tyr4Ter
ENST00000525526.2:c.12T>A
ENSP00000437575.1:p.Tyr4Ter
ENST00000383070.1:c.12T>A
ENSP00000372547.1:p.Tyr4Ter

Variation displays