Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.45 (T)
Location

Chromosome 15:88855374 (forward strand) | View in location tab

Co-located

with COSMIC COSM146361 (G/T), COSM3927718 (G/T)

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs52808766, rs59582752

This variant has 11 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 3841 sample genotypes.

Variant displays