Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2655436 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM098079, CM930696

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_011_SRY_480000_0013, 8618

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

Y:g.2655436C>T
ENST00000534739.2:c.209G>A
ENSP00000438917.1:p.Trp70Ter
ENST00000525526.2:c.209G>A
ENSP00000437575.1:p.Trp70Ter
ENST00000383070.1:c.209G>A
ENSP00000372547.1:p.Trp70Ter

Variation displays