Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/- | Ancestral: A

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


with COSMIC COSM1735994 (A/-)

Most severe consequence
Evidence status

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

About this variant

This variant overlaps 4 transcripts and has 7 individual genotypes.

Variation displays