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]

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

Chromosome 3:41224606 (forward strand) | View in location tab


with COSMIC COSM5661 (G/T), COSM5668 (G/C), COSM5672 (G/A)

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, is associated with 5 phenotypes and is mentioned in 1 citation.

Variation displays