Most severe consequence
 
intron variant
Alleles
G/T
Location

Supercontig scaffold_00062:948795 (forward strand)|VCF:scaffold_00062  948795  tmp_scaffold_00062_948795_G_T  G  T

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 1 sample genotype.

Variant displays