Original source

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

Alleles
C/A/T | Ancestral: C | Ambiguity code: H
Location

Chromosome 4:186210508 (forward strand) | View in location tab

Co-located

with COSMIC COSM586929 (C/T) ; HGMD-PUBLIC CM053829

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NM_207352.3:c.1445C>A

This variation has 14 HGVS names - click the plus to show

Variation displays