Original source

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

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

Chromosome 17:7673766 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5934

This variation has 71 HGVS names - click the plus to show

Variation displays