Original source

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

Alleles
T/C|Ambiguity code: Y
Location

Chromosome 18:17731274 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Synonyms

ENSEMBL:STAR-4strain ENSRNOSNP2783225

HGVS name

18:g.17731274T>C

About this variant

This variant has 1 sample genotype.

Variant displays