Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 6:43604627 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

LSDB POLH_p.Y299X

This variation has 13 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts, has 2504 individual genotypes and is mentioned in 1 citation.

Variation displays