Original source

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

Alleles
T/G|Ambiguity code: K
Location

Chromosome 2:142196869 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays