Original source

Variation features from dbSNP (release 125) | [View in dbSNP]

Alleles
T/A | Ambiguity code: W
Location

Chromosome 2L:39220938 (reverse strand) | View in location tab

Most severe consequence
HGVS name

2L:g.39220938A>T

About this variant

This variant overlaps 5 transcripts and has 2 individual genotypes.

Variation displays