Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome Y:2787278 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920651

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_002_SRY_480000_0003, 8608

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

Y:g.2787278A>G
ENST00000623823.1:c.326T>C
ENSP00000485519.1:p.Phe109Ser
ENST00000383070.1:c.326T>C
ENSP00000372547.1:p.Phe109Ser

Variation displays