Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.06 (G)
Location

Chromosome 16:47663707 (forward strand) | View in location tab

Co-located

with COSMIC COSM1629903 (A/T), COSM1629904 (A/T), COSM1629902 (A/T) ; HGMD-PUBLIC CM031328

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

This variant has 10 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 3157 sample genotypes.

Variant displays