Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

Chromosome 2:113246853 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM981477

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_100_PAX8_167415_0003, 4516

This variation has 22 HGVS names - click the plus to show

2:g.113246853C>T
ENST00000263334.6:c.92G>A
ENSP00000263334.6:p.Arg31His
ENST00000436293.3:n.355-3914C>T
ENST00000429538.4:c.92G>A
ENSP00000395498.3:p.Arg31His
ENST00000556070.2:n.35+11283C>T
ENST00000263335.8:c.92G>A
ENSP00000263335.7:p.Arg31His
ENST00000451179.2:n.165-8537C>T
ENST00000397647.4:c.92G>A
ENSP00000380768.3:p.Arg31His
ENST00000616073.1:n.142-8537C>T
ENST00000348715.6:c.92G>A
ENSP00000314750.5:p.Arg31His
ENST00000445745.2:n.378-8537C>T
ENST00000422956.3:n.36-8537C>T
ENST00000617509.1:n.152-8537C>T
ENST00000467778.2:n.256G>A
ENST00000333145.6:n.133-8537C>T
ENST00000553869.3:n.154+8641C>T
ENST00000554830.1:c.26-4075G>A

Variation displays