Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/T
Location

Chromosome 16: between 88425485 and 88425486 (forward strand) | View in location tab

Most severe consequence
HGVS name

16:g.88425485_88425486insT

About this variant

This variant overlaps 2 transcripts.

Variation displays