Original source

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

Alleles
A/G | Ambiguity code: R
Location

Chromosome Y:2655319 (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 7 HGVS names - click the plus to show

Y:g.2655319A>G
ENST00000534739.2:c.326T>C
ENSP00000438917.1:p.Phe109Ser
ENST00000525526.2:c.326T>C
ENSP00000437575.1:p.Phe109Ser
ENST00000383070.1:c.326T>C
ENSP00000372547.1:p.Phe109Ser

Variation displays