Original source

Variants (including SNPs and indels) imported from dbSNP [mapped to the assembly Nleu1.0] (release 145)|View in dbSNP

Alleles
C/G|Ambiguity code: S
Location

Contig ADFV01162226.1:2148 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Synonyms

ENSEMBL ENSNLESNP1

HGVS name

ADFV01162226.1:g.2148C>G

About this variant

This variant has 1 sample genotype.

Variant displays