Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 2:178453570 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM062579

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 16688

This variation has 8 HGVS names - click the plus to show

2:g.178453570C>T
ENST00000442710.4:c.3C>T
ENSP00000410776.1:p.Thr2Ile
ENST00000375129.7:c.161C>T
ENSP00000364271.4:p.Thr54Ile
ENST00000409117.6:c.161C>T
ENSP00000386647.3:p.Thr54Ile
ENST00000437056.4:n.320C>T

About this variant

This variant overlaps 17 transcripts and is associated with 2 phenotypes.

Variation displays