Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 3:122284317 (forward strand) | View in location tab

Co-located

with COSMIC COSM479299 (T/A) ; HGMD-PUBLIC CM980304 ; PhenCode CASRdb_c.2363T>G (T/G)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_043_CASR_601199_0027, 9992

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

Variation displays