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]

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

Chromosome 3:41224622 (forward strand) | View in location tab


with COSMIC COSM5666 (C/A), COSM5679 (C/G), COSM5662 (C/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 11 synonyms - click the plus to show

This variation has 60 HGVS names - click the plus to show

About this variant

This variant overlaps 33 transcripts and is associated with 6 phenotypes.

Variation displays