This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/A/C/G | Ancestral: T | Ambiguity code: N | MAF: 0.48 (T)

Chromosome 11:17520892 (forward strand) | View in location tab


with COSMIC COSM4145599 (T/C), COSM4145600 (T/C)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 36 HGVS names - Show

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 24 transcripts, has 3733 sample genotypes and is associated with 1 phenotype.

Variant displays