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 4:55152093 (forward strand) | View in location tab

Co-located

with COSMIC COSM736 (A/T)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 4741, Cosmic:736

This variation has 5 HGVS names - click the plus to show

Variation displays