Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to Rnor_6.0) (release 138) | View in dbSNP

Alleles
T/A | Ambiguity code: W
Location

Chromosome 1:113728121 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Synonyms

ENSEMBL:celera ENSRNOSNP11773

HGVS name

1:g.113728121T>A

About this variant

This variant has 1 sample genotype.

Variant displays