Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)

Chromosome 16:88643420 (forward strand) | View in location tab


with COSMIC COSM3749388 (A/G)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 13 transcripts, has 1163 individual genotypes and is mentioned in 1 citation.

Variation displays