Original source

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

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

Chromosome 6:43572364 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB POLH_p.Y299X

This variation has 16 HGVS names - click the plus to show

Variation displays