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

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

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

Co-located

with COSMIC COSM436669 (C/T)

Most severe consequence
Clinical significance

Synonyms

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

Variation displays