This variation has been flagged

Flagged as suspect by dbSNP

Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 5:228396 (forward strand) | View in location tab

Co-located

with COSMIC COSM247233 (G/C)

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

Variation displays