Original source

Variants (including SNPs and indels) imported from dbSNP [remapped to Felis_catus-6.2] (release 144) | View in dbSNP

G/A | Ambiguity code: R

Chromosome A1:10132487 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 2 transcripts.

Variant displays