Original source

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

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

Chromosome 17:7674220 (forward strand) | View in location tab


with COSMIC COSM340107 (C/G), COSM241996 (C/A), COSM99021 (C/T), COSM1646858 (C/G), COSM1646857 (C/A), COSM1640830 (C/T), COSM3378346 (C/A), COSM3356964 (C/T), COSM340106 (C/G), COSM241994 (C/A), COSM99020 (C/T), COSM241995 (C/A), COSM99602 (C/T), COSM340105 (C/G), COSM46135 (C/-), COSM6549 (C/A), COSM11491 (C/G), COSM10662 (C/T) ; HGMD-PUBLIC CM920675 ; PhenCode TP53_g.13380del (C/-), TP53_g.13380G>A (C/T), TP53_g.13380G>T (C/A), TP53_g.13380G>C (C/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 74 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12

About this variant

This variant overlaps 42 transcripts, is associated with 4 phenotypes and is mentioned in 4 citations.

Variation displays