Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (G)
Location

Chromosome 4:73869527 (forward strand) | View in location tab

Co-located

with COSMIC COSM3749883 (A/G)

Most severe consequence
Evidence status

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2541 individual genotypes.

Variation displays