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

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

Chromosome 12:25380276 (forward strand) | View in location tab


with COSMIC COSM551 (T/G), COSM552 (T/C), COSM553 (T/A), COSM1667042 (T/A), COSM1140131 (T/A), COSM1158660 (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