This variation has been flagged

Variation has more than 3 different alleles

Original source

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

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

Chromosome 7:55174014 (forward strand) | View in location tab

Co-located

with COSMIC COSM6253 (G/T), COSM6252 (G/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 6 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

Variation displays