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 3:181712889 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM030718

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_201_SOX2_184429_0001, 5459

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

3:g.181712889C>T
ENST00000498731.4:n.564-2296C>T
ENST00000593549.4:n.290-2296C>T
ENST00000493521.4:n.782+13006C>T
ENST00000477928.1:n.391+13006C>T
ENST00000595084.2:n.289+13006C>T
ENST00000596250.4:n.289+13006C>T
ENST00000630887.1:n.289+13006C>T
ENST00000600386.4:n.290-2296C>T
ENST00000626299.1:n.290-2296C>T
ENST00000598474.2:n.289+13006C>T
ENST00000476964.4:n.482-26680C>T
ENST00000629552.1:n.266-2296C>T
ENST00000627501.1:n.289+13006C>T
ENST00000626619.1:n.266-2296C>T
ENST00000600801.4:n.290-2296C>T
ENST00000629781.1:n.290-2296C>T
ENST00000597651.4:n.289+13006C>T
ENST00000595287.1:n.286+13006C>T
ENST00000597828.4:n.638-2296C>T
ENST00000593330.1:n.44+13006C>T
ENST00000600778.2:n.285+13006C>T
ENST00000628343.1:n.289+13006C>T
ENST00000492337.4:n.739-2296C>T
ENST00000466034.4:n.389-2296C>T
ENST00000630553.1:n.285+13006C>T
ENST00000491282.4:n.577+13006C>T
ENST00000498226.4:n.287-77784C>T
ENST00000628496.1:n.290-2296C>T
ENST00000628810.1:n.48-2296C>T
ENST00000629112.1:n.290-2296C>T
ENST00000599082.1:n.50+13245C>T
ENST00000629830.1:n.289+13006C>T
ENST00000469278.4:n.473-26680C>T
ENST00000325404.2:c.529C>T
ENSP00000323588.1:p.Gln177Ter
ENST00000627738.1:n.23+11440C>T
ENST00000627530.1:n.290-2296C>T
LRG_719:g.5956C>T
LRG_719t1:c.529C>T
LRG_719p1:p.Gln177Ter

About this variant

This variant overlaps 42 transcripts and is associated with 2 phenotypes.

Variation displays