Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 3:181712581 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM061213

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5466, 2010_April_001_207_SOX2_184429_0008

This variant has 41 HGVS names - click the plus to show

3:g.181712581G>C
ENST00000498731.5:n.564-2604G>C
ENST00000593549.5:n.290-2604G>C
ENST00000493521.5:n.782+12698G>C
ENST00000595084.2:n.289+12698G>C
ENST00000477928.1:n.391+12698G>C
ENST00000596250.5:n.289+12698G>C
ENST00000600386.5:n.290-2604G>C
ENST00000630887.2:n.289+12698G>C
ENST00000626299.2:n.290-2604G>C
ENST00000598474.3:n.289+12698G>C
ENST00000476964.5:n.482-26988G>C
ENST00000629552.2:n.266-2604G>C
ENST00000627501.2:n.289+12698G>C
ENST00000626619.2:n.266-2604G>C
ENST00000600801.5:n.290-2604G>C
ENST00000629781.2:n.290-2604G>C
ENST00000597651.5:n.289+12698G>C
ENST00000595287.1:n.286+12698G>C
ENST00000597828.5:n.638-2604G>C
ENST00000593330.1:n.44+12698G>C
ENST00000600778.3:n.285+12698G>C
ENST00000628343.2:n.289+12698G>C
ENST00000492337.5:n.739-2604G>C
ENST00000466034.5:n.389-2604G>C
ENST00000630553.1:n.285+12698G>C
ENST00000491282.5:n.577+12698G>C
ENST00000628496.2:n.290-2604G>C
ENST00000498226.5:n.287-78092G>C
ENST00000599082.1:n.50+12937G>C
ENST00000629112.2:n.290-2604G>C
ENST00000628810.1:n.48-2604G>C
ENST00000325404.2:c.221G>C
ENSP00000323588.1:p.Arg74Pro
ENST00000469278.5:n.473-26988G>C
ENST00000627738.1:n.23+11132G>C
ENST00000629830.2:n.289+12698G>C
ENST00000627530.2:n.290-2604G>C
LRG_719:g.5648G>C
LRG_719t1:c.221G>C
LRG_719p1:p.Arg74Pro

About this variant

This variant overlaps 41 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays