Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (T)
Location

Chromosome 1:158685251 (forward strand) | View in location tab

Co-located

with COSMIC COSM1499094 (G/C) ; HGMD-PUBLIC CM890106

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 5431

This variation has 11 HGVS names - click the plus to show

Variation displays