Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome 17:7577538 (forward strand) | View in location tab


with COSMIC COSM6549 (C/A), COSM10662 (C/T), COSM11491 (C/G), COSM46135 (C/-), COSM99602 (C/T), COSM241995 (C/A), COSM340105 (C/G), COSM99020 (C/T), COSM340106 (C/G), COSM241994 (C/A), COSM1640830 (C/T), COSM1646858 (C/G), COSM1646857 (C/A), COSM99021 (C/T), COSM340107 (C/G), COSM241996 (C/A) ; HGMD-PUBLIC CM920675 ; PhenCode TP53_g.13380G>A (C/T), TP53_g.13380G>T (C/A), TP53_g.13380G>C (C/G), TP53_g.13380del (C/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 37 HGVS names - click the plus to show

Variation displays