Original source

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

Alleles
-/AAT
Location

Chromosome 5: between 181236638 and 181236639 (forward strand) | View in location tab

Most severe consequence
Synonyms
HGVS name

5:g.181236638_181236639insAAT

About this variant

This variant overlaps 42 transcripts.

Variation displays