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: 0.43 (C)

Chromosome 16:3254654 (forward strand) | View in location tab


with COSMIC COSM3754870 (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 17 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 1117 individual genotypes, is associated with 2 phenotypes and is mentioned in 4 citations.

Variation displays