Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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


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

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 42 transcripts, is associated with 4 phenotypes and is mentioned in 1 citation.

Variant displays