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 17:43124016 (forward strand) | View in location tab


with COSMIC COSM3734724 (C/A), COSM436669 (C/T)

Most severe consequence
Clinical significance


LSDB U14680.1:c.80+1G>T, U14680.1:c.80+1G>C, U14680.1:c.80+1G>A

This variation has 72 HGVS names - click the plus to show

About this variant

This variant overlaps 78 transcripts and is associated with 4 phenotypes.

Variation displays