Original source

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

A/T | Ancestral: A | Ambiguity code: W

Chromosome 17:7674193 (forward strand) | View in location tab


with COSMIC COSM3378343 (A/G), COSM4139864 (A/T), COSM3378344 (A/G), COSM4139865 (A/T), COSM1386606 (A/G), COSM1230109 (A/T), COSM1386605 (A/G), COSM1230108 (A/T), COSM43530 (A/T), COSM43842 (A/G), COSM44890 (A/C) ; HGMD-PUBLIC CD941800, CM941332 ; PhenCode TP53_g.13407T>C (A/G), TP53_g.13407T>A (A/T), TP53_g.13407T>G (A/C), TP53_g.13407del (A/-)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 72 HGVS names - click the plus to show

About this variant

This variant overlaps 42 transcripts and is associated with 3 phenotypes.

Variation displays