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 | MAF: < 0.01 (T)

Chromosome 17:7673802 (forward strand) | View in location tab


with COSMIC COSM1646808 (C/G), COSM1645335 (C/T), COSM1640828 (C/A), COSM3675521 (C/A), COSM3356963 (C/T), COSM165077 (C/G), COSM99729 (C/T), COSM318169 (C/A), COSM10779 (C/A), COSM44440 (C/-), COSM43896 (C/G), COSM10660 (C/T) ; HGMD-PUBLIC CM920677, CM010472, CM004342 ; PhenCode TP53_g.13798G>A (C/T), TP53_g.13798G>T (C/A), TP53_g.13798G>C (C/G), TP53_g.13798del (C/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: HumanCoreExome-12

Variation displays