Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 14:88384576 (forward strand) | View in location tab

Most severe consequence
HGVS name

14:g.88384576T>G

About this variant

This variant overlaps 18 transcripts.

Variation displays