Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2787267 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930700

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_007_SRY_480000_0009, 8614

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

Y:g.2787267C>T
ENST00000623823.1:c.337G>A
ENSP00000485519.1:p.Ala113Thr
ENST00000383070.1:c.337G>A
ENSP00000372547.1:p.Ala113Thr

Variation displays