This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: < 0.01 (T)
Location

Chromosome 16:3254380 (forward strand) | View in location tab

Co-located

with COSMIC COSM1214873 (C/A), COSM970394 (C/T) ; HGMD-PUBLIC CM012151

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 69 HGVS names - click the plus to show

About this variant

This variant overlaps 45 transcripts, has 2504 sample genotypes and is associated with 3 phenotypes.

Variant displays