Original source

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

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

Chromosome 17:7577084 (forward strand) | View in location tab

Co-located

with COSMIC COSM44227 (T/A), COSM45649 (T/C), COSM43614 (T/G), COSM131484 (T/C), COSM131474 (T/A) ; HGMD-PUBLIC CM083790 ; PhenCode TP53_g.13834A>T (T/A), TP53_g.13834A>G (T/C), TP53_g.13834A>C (T/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5934

This variation has 34 HGVS names - click the plus to show

Variation displays