Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome Y:2787395 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930696, CM098079

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_011_SRY_480000_0013, 8618

This variation has 3 HGVS names - click the plus to show

Y:g.2787395C>T
ENST00000383070.1:c.209G>A
ENSP00000372547.1:p.Trp70Ter

Variation displays