Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2655592 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981859

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8626, 2010_April_001_017_SRY_480000_0021

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

Y:g.2655592C>T
ENST00000534739.2:c.53G>A
ENSP00000438917.1:p.Ser18Asn
ENST00000525526.2:c.53G>A
ENSP00000437575.1:p.Ser18Asn
ENST00000383070.1:c.53G>A
ENSP00000372547.1:p.Ser18Asn

Variation displays