Original source

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

G/A/C | Ancestral: G | Ambiguity code: V

Chromosome 9:72816161 (forward strand) | View in location tab


with COSMIC COSM1462918 (G/A), COSM1288480 (G/T) ; HGMD-PUBLIC CM020521, CM070292

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and is associated with 4 phenotypes.

Variation displays