Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/A/T | Ancestral: C | Ambiguity code: H

Chromosome 4:47403391 (forward strand) | View in location tab


with COSMIC COSM3604134 (C/T)

Most severe consequence
Synonymous variant
Evidence status

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 270 sample genotypes.

Variant displays