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 2:98395999 (forward strand) | View in location tab

Co-located

with COSMIC COSM1248533 (C/T) ; HGMD-PUBLIC CM014538, CM104556

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8884, 2010_April_001_023_CNGA3_600053_0009

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

2:g.98395999C>T
ENST00000409937.1:c.841C>T
ENSP00000386761.1:p.Arg281Cys
ENST00000436404.3:c.775C>T
ENSP00000410070.2:p.Arg259Cys
ENST00000393504.2:c.829C>T
ENSP00000377140.1:p.Arg277Cys
ENST00000272602.3:c.829C>T
ENSP00000272602.2:p.Arg277Cys

Variation displays