Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/G | Ambiguity code: S
Location

Chromosome Y:2787321 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930699

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8621, 2010_April_001_013_SRY_480000_0016

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

Y:g.2787321C>G
ENST00000383070.1:c.283G>C
ENSP00000372547.1:p.Gly95Arg

About this variant

This variant overlaps 4 transcripts and is associated with 2 phenotypes.

Variation displays