Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Stop gained
Evidence status

Synonyms

LSDB POLH_p.Y299X

HGVS names

This variant has 16 HGVS names - Show

About this variant

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

Variant displays