Original source

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

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 2:208248389 (forward strand) | View in location tab


with COSMIC COSM28749 (G/C), COSM28747 (G/A), COSM28748 (G/T)

Most severe consequence
Missense variant

This variant has 3 synonyms - click the plus to show

This variant has 34 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts.

Variant displays