Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (C)

Chromosome 4:146639259 (forward strand) | View in location tab


with COSMIC COSM3760418 (T/C)

Most severe consequence
Evidence status


Uniprot VAR_059321

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

This variation has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2271 individual genotypes.

Variation displays