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 1:197477806 (forward strand) | View in location tab

Co-located

with COSMIC COSM3385589 (G/A) ; HGMD-PUBLIC CM043275

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_022983

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

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 6 transcripts, has 2504 individual genotypes and is associated with 1 phenotype.

Variation displays