Original source

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

Alleles
G/C | Ambiguity code: S
Location

Chromosome Y:2787334 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920647

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8611, 2010_April_001_005_SRY_480000_0006

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

Y:g.2787334G>C
ENST00000623823.1:c.270C>G
ENSP00000485519.1:p.Ile90Met
ENST00000383070.1:c.270C>G
ENSP00000372547.1:p.Ile90Met

Variation displays