Original source

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

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

Chromosome 2:234675806 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM920701

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_127_UGT1A1_191740_0003, 5989

This variation has 39 HGVS names - click the plus to show

2:g.234675806C>T
ENST00000373445.1:c.982C>T
ENSP00000362544.1:p.Gln328Ter
ENST00000305139.6:c.988C>T
ENSP00000303174.6:p.Gln330Ter
ENST00000373409.3:c.994C>T
ENSP00000362508.3:p.Gln332Ter
ENST00000482026.1:c.994C>T
ENSP00000418532.1:p.Gln332Ter
ENST00000446481.2:c.187C>T
ENSP00000401541.1:p.Gln63Ter
ENST00000373424.1:c.187C>T
ENSP00000362523.1:p.Gln63Ter
ENST00000608383.1:c.991C>T
ENSP00000476741.1:p.Gln331Ter
ENST00000608381.1:c.994C>T
ENSP00000477394.1:p.Gln332Ter
ENST00000373426.3:c.982C>T
ENSP00000362525.3:p.Gln328Ter
ENST00000450233.1:c.994C>T
ENSP00000408608.1:p.Gln332Ter
ENST00000609637.1:c.982C>T
ENSP00000476286.1:p.Gln328Ter
ENST00000360418.3:c.991C>T
ENSP00000353593.3:p.Gln331Ter
ENST00000609767.1:c.994C>T
ENSP00000476805.1:p.Gln332Ter
ENST00000373414.3:c.994C>T
ENSP00000362513.3:p.Gln332Ter
ENST00000406651.1:c.187C>T
ENSP00000386107.1:p.Gln63Ter
ENST00000305208.5:c.991C>T
ENSP00000304845.5:p.Gln331Ter
ENST00000344644.5:c.982C>T
ENSP00000343838.5:p.Gln328Ter
ENST00000373450.4:c.982C>T
ENSP00000362549.4:p.Gln328Ter
ENST00000354728.4:c.982C>T
ENSP00000346768.4:p.Gln328Ter

Variation displays