Original source

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

Alleles
-/T
Location

Chromosome 13: between 19957146 and 19957147 (forward strand) | View in location tab

Most severe consequence
HGVS name

13:g.19957146_19957147insT

About this variant

This variant overlaps 6 transcripts.

Variation displays