Original source

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

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

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

Co-located

with COSMIC 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 8 chips - click the plus to show

Variation displays