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

Chromosome 14:24259769 (forward strand) | View in location tab

Co-located

with COSMIC COSM183539 (G/A) ; HGMD-PUBLIC CM065480, CM012196

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 28 transcripts, has 2504 individual genotypes and is associated with 3 phenotypes.

Variation displays