Original source

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

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

Chromosome 6:161785820 (forward strand) | View in location tab

Co-located

with COSMIC COSM1722444 (G/A), COSM1722445 (G/A) ; HGMD-PUBLIC CM991007

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 15 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ImmunoChip, Illumina_ExomeChip

About this variant

This variant overlaps 7 transcripts, has 2505 sample genotypes, is associated with 4 phenotypes and is mentioned in 2 citations.

Variant displays