Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N

Chromosome 18:48591918 (forward strand) | View in location tab


with COSMIC COSM14140 (C/T), COSM1158192 (C/G), COSM14151 (C/A) ; HGMD-PUBLIC CM981228, CM040450, CM041789

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 36 HGVS names - click the plus to show

Variation displays