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

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 - click the plus to show

This variant has 21 HGVS names - click the plus to show

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 24 transcripts, has 2572 sample genotypes and is associated with 1 phenotype.

Variant displays