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 4:55141036 (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 7 HGVS names - click the plus to show

Variation displays