Original source

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

Alleles
T/A | Ambiguity code: W
Location

Chromosome Y:2655328 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920650

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8612, 2010_April_001_006_SRY_480000_0007

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

Y:g.2655328T>A
ENST00000534739.2:c.317A>T
ENSP00000438917.1:p.Lys106Ile
ENST00000525526.2:c.317A>T
ENSP00000437575.1:p.Lys106Ile
ENST00000383070.1:c.317A>T
ENSP00000372547.1:p.Lys106Ile

Variation displays