Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 2:233767161 (forward strand) | View in location tab

Co-located

with COSMIC COSM301335 (A/C), COSM301329 (A/C), COSM301328 (A/C), COSM301333 (A/C), COSM301331 (A/C), COSM301332 (A/C), COSM301334 (A/C), COSM301330 (A/C), COSM301327 (A/C) ; HGMD-PUBLIC CM930723

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_129_UGT1A1_191740_0005, 5991

This variation has 36 HGVS names - click the plus to show

2:g.233767161A>G
ENST00000373445.1:c.983A>G
ENSP00000362544.1:p.Gln328Arg
ENST00000373409.4:c.995A>G
ENSP00000362508.3:p.Gln332Arg
ENST00000305139.7:c.989A>G
ENSP00000303174.6:p.Gln330Arg
ENST00000482026.2:c.995A>G
ENSP00000418532.1:p.Gln332Arg
ENST00000373424.2:c.188A>G
ENSP00000362523.1:p.Gln63Arg
ENST00000446481.3:c.188A>G
ENSP00000401541.1:p.Gln63Arg
ENST00000373426.3:c.983A>G
ENSP00000362525.3:p.Gln328Arg
ENST00000450233.1:c.995A>G
ENSP00000408608.1:p.Gln332Arg
ENST00000360418.4:c.992A>G
ENSP00000353593.3:p.Gln331Arg
ENST00000609767.2:c.995A>G
ENSP00000476805.2:p.Gln332Arg
ENST00000373414.3:c.995A>G
ENSP00000362513.3:p.Gln332Arg
ENST00000406651.1:c.188A>G
ENSP00000386107.1:p.Gln63Arg
ENST00000305208.6:c.992A>G
ENSP00000304845.5:p.Gln331Arg
ENST00000373450.4:c.983A>G
ENSP00000362549.4:p.Gln328Arg
ENST00000344644.6:c.983A>G
ENSP00000343838.5:p.Gln328Arg
ENST00000354728.4:c.983A>G
ENSP00000346768.4:p.Gln328Arg
LRG_733:g.11889A>G
LRG_733t1.1:c.992A>G
LRG_733p1.1:p.Gln331Arg

Variation displays