Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.20 (G)
Location

Chromosome 9:712156 (forward strand) | View in location tab

Co-located

with COSMIC COSM150570 (T/G), COSM3927869 (T/G), COSM3927868 (T/G)

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

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 6 transcripts and has 4072 sample genotypes.

Variant displays