Original source

Variation features from DPGP, with Ensembl identifiers (release 1) | DPGP 1

G/A/C/T | Ambiguity code: N

Chromosome 2L:1056714 (forward strand) | View in location tab

Most severe consequence
Intron variant
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 23 sample genotypes.

Variant displays