Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.40 (G)

Chromosome 17:7676154 (forward strand) | View in location tab


with COSMIC COSM3766191 (G/C), COSM3766192 (G/C), COSM3766193 (G/C), COSM3766190 (G/C), COSM45985 (G/A), COSM250061 (G/C) ; HGMD-PUBLIC CM961374 ; PhenCode TP53_g.11446del (G/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 10 synonyms - click the plus to show

This variation has 55 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 42 transcripts, has 1829 individual genotypes, is associated with 5 phenotypes and is mentioned in 197 citations.

Variation displays