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 3:41224646 (forward strand) | View in location tab


with COSMIC COSM5667 (C/T), COSM5692 (C/A), COSM5689 (C/G), COSM6100 (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 2 phenotypes.

Variation displays