This variation has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 3:41266101 (forward strand) | View in location tab


with COSMIC COSM5673 (C/A), COSM5677 (C/G), COSM5669 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 9 synonyms - click the plus to show

This variation has 60 HGVS names - click the plus to show

Variation displays