Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 4:187113158 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM041495

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 15845, NM_207352.3:c.181G>A

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

4:g.187113158G>A
ENST00000378802.4:c.181G>A
ENSP00000368079.4:p.Gly61Ser

Variation displays