Original source

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

Alleles
C/T | Ambiguity code: Y
Location

Chromosome 12:52680896 (forward strand) | View in location tab

Co-located

with COSMIC COSM162065 (C/T) ; HGMD-PUBLIC CM970851 ; PhenCode HIFD_KRT81:c.1237G>A (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

12:g.52680896C>T
ENST00000423955.2:c.-5+11166C>T
ENST00000544024.1:c.-4-14801C>T
ENST00000553310.2:c.-4-14801C>T
ENST00000327741.5:c.1237G>A
ENSP00000369349.4:p.Glu413Lys

Variation displays