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

Chromosome 12:25227342 (forward strand) | View in location tab

Co-located

with COSMIC COSM3688142 (T/G), COSM1158660 (T/C), COSM1140131 (T/A), COSM553 (T/A), COSM551 (T/G), COSM552 (T/C)

Most severe consequence
Clinical significance

This variation has 5 synonyms - click the plus to show

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

Variation displays