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 2:128183754 (forward strand) | View in location tab

Co-located

with COSMIC COSM1287402 (C/T) ; HGMD-PUBLIC CM951006

Most severe consequence
Clinical significance

Synonyms

LSDB 17264

This variation has 11 HGVS names - click the plus to show

2:g.128183754C>T
ENST00000402125.2:c.121-2179C>T
ENST00000409048.1:c.731C>T
ENSP00000386679.1:p.Pro244Leu
ENST00000464089.1:n.215C>T
ENST00000453608.2:c.794C>T
ENSP00000404030.2:p.Pro265Leu
ENST00000422777.3:c.629C>T
ENSP00000409543.3:p.Pro210Leu
ENST00000234071.3:c.629C>T
ENSP00000234071.3:p.Pro210Leu

Variation displays