Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 7:128252162 (forward strand) | View in location tab


with HGMD-PUBLIC CS982252

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12

About this variant

This variant overlaps 2 transcripts.

Variant displays