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 2:98389696 (forward strand) | View in location tab

Co-located

with COSMIC COSM3673768 (C/A) ; HGMD-PUBLIC CM980374

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 8876, 2010_April_001_016_CNGA3_600053_0001

This variation has 10 HGVS names - click the plus to show

2:g.98389696C>T
ENST00000393503.2:n.493C>T
ENST00000409937.1:c.500C>T
ENSP00000386761.1:p.Pro167Leu
ENST00000436404.4:c.434C>T
ENSP00000410070.2:p.Pro145Leu
ENST00000393504.3:c.488C>T
ENSP00000377140.1:p.Pro163Leu
ENST00000272602.4:c.488C>T
ENSP00000272602.2:p.Pro163Leu

Variation displays