Original source

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

Alleles
A/- | Ancestral: A
Location

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

Co-located

with COSMIC COSM1735994 (A/-)

Most severe consequence

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 6 individual genotypes.

Variation displays