Original source

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

G/A | Ancestral: G | Ambiguity code: R

Chromosome 17:7674241 (forward strand) | View in location tab


with COSMIC COSM10709 (G/C), COSM10812 (G/A), COSM10935 (G/T), COSM44657 (G/-), COSM214171 (G/A), COSM437501 (G/C), COSM1230110 (G/T), COSM1230111 (G/T), COSM214170 (G/A), COSM437502 (G/C), COSM3712577 (G/T), COSM3362448 (G/C), COSM3522695 (G/A), COSM2744620 (G/T), COSM1649402 (G/A), COSM2744619 (G/C), COSM214172 (G/A), COSM437503 (G/C), COSM1230112 (G/T) ; HGMD-PUBLIC CM920673 ; PhenCode TP53_g.13359C>G (G/C), TP53_g.13359C>T (G/A), TP53_g.13359del (G/-), TP53_g.13359C>A (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

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

About this variant

This variant overlaps 42 transcripts, is associated with 6 phenotypes and is mentioned in 2 citations.

Variant displays