Original source

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

A/- | Ancestral: A

Chromosome 12:90978266 (forward strand) | View in location tab


with COSMIC COSM1735994 (A/-)

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 6 sample genotypes.

Variant displays