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]

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

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


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

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

About this variant

This variant overlaps 12 transcripts and is associated with 2 phenotypes.

Variation displays