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 4:54274869 (forward strand) | View in location tab

Co-located

with COSMIC COSM1430077 (T/C), COSM739 (T/A) ; HGMD-PUBLIC CM074406

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:739, 4744

This variation has 10 HGVS names - click the plus to show

Variation displays