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 3:41266125 (forward strand) | View in location tab

Co-located

with COSMIC COSM5701 (C/G), COSM5730 (C/A), COSM5676 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 20 HGVS names - click the plus to show

Variation displays