Original source

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

G/C/T | Ancestral: G | Ambiguity code: B

Chromosome 4:54101631 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 32 sample genotypes.

Variant displays