Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 9:75431077 (forward strand) | View in location tab


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

Most severe consequence
Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 18 HGVS names - click the plus to show

Variation displays