Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 17:7577511 (forward strand) | View in location tab

Co-located

with COSMIC COSM44890 (A/C), COSM43530 (A/T), COSM43842 (A/G), COSM1230108 (A/T), COSM1386605 (A/G), COSM1230109 (A/T), COSM1386606 (A/G) ; 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 35 HGVS names - click the plus to show

Variation displays