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]

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

Chromosome 3:41224607 (forward strand) | View in location tab


with COSMIC COSM5681 (A/G), COSM5691 (A/T), COSM5690 (A/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 7 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 3 phenotypes.

Variation displays