Original source

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

Alleles
C/T|Ambiguity code: Y
Location

Contig ADFV01162869.1:2416 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Synonyms

ENSEMBL ENSNLESNP73

HGVS name

ADFV01162869.1:g.2416C>T

About this variant

This variant has 1 sample genotype.

Variant displays