Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/G | Ancestral: C | Ambiguity code: S

Chromosome 5:150053482 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 8 transcripts and 1 regulatory feature.

Variant displays