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 17:37822015 (forward strand) | View in location tab

Co-located

with COSMIC COSM1610160 (C/A) ; HGMD-PUBLIC CM000576 ; PhenCode TCAP:c.157C>T (C/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_220_TCAP_604488_0001, 12687

This variation has 8 HGVS names - click the plus to show

Variation displays