Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:7673776 (forward strand) | View in location tab

Co-located

with COSMIC COSM1725698 (G/C), COSM1636702 (G/A), COSM3378339 (G/A), COSM3675520 (G/C), COSM99934 (G/C), COSM99925 (G/A), COSM43813 (G/-), COSM44918 (G/T), COSM10992 (G/C), COSM10704 (G/A) ; HGMD-PUBLIC CM920678, CM056413 ; PhenCode TP53_g.13824C>T (G/A), TP53_g.13824C>G (G/C), TP53_g.13824C>A (G/T), TP53_g.13824del (G/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 71 HGVS names - click the plus to show

Variation displays