Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: < 0.01 (A)
Location

Chromosome 2:27131672 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1019527

Most severe consequence
 
Splice donor variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 17 transcripts and has 2504 sample genotypes.

Variant displays