Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 1:169529939 (forward strand) | View in location tab

Co-located

with COSMIC COSM677256 (C/T) ; HGMD-PUBLIC CM032567

Most severe consequence
Clinical significance

Synonyms

LSDB 17297

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

1:g.169529939C>A
ENST00000367796.3:c.439G>T
ENSP00000356770.3:p.Glu147Ter
ENST00000546081.1:c.28G>T
ENSP00000439664.1:p.Glu10Ter
ENST00000367797.3:c.439G>T
ENSP00000356771.3:p.Glu147Ter

Variation displays