Original source

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

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

Chromosome 2:98396042 (forward strand) | View in location tab

Co-located

with COSMIC COSM1669158 (C/T) ; HGMD-PUBLIC CM980377

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8880, 2010_April_001_020_CNGA3_600053_0005

This variation has 9 HGVS names - click the plus to show

2:g.98396042C>G
ENST00000409937.1:c.884C>G
ENSP00000386761.1:p.Thr295Arg
ENST00000436404.3:c.818C>G
ENSP00000410070.2:p.Thr273Arg
ENST00000393504.2:c.872C>G
ENSP00000377140.1:p.Thr291Arg
ENST00000272602.3:c.872C>G
ENSP00000272602.2:p.Thr291Arg

Variation displays