Original source

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

Alleles
C/T/G | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (T)
Location

Chromosome 16:3254380 (forward strand) | View in location tab

Co-located

with COSMIC COSM1214873 (C/A), COSM970394 (C/T) ; HGMD-PUBLIC CM012151

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 46 HGVS names - click the plus to show

Variation displays