Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/A|Ancestral: G|Ambiguity code: R

Chromosome 10:70600713 (forward strand)|View in location tab

Co-located variants

COSMIC COSM386287 ; HGMD-PUBLIC CM992949 ; PhenCode PRF1base_D0067:g.3463C>T (G/A)

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB 2010_April_001_079_PRF1_170280_0003, 4588

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and is associated with 2 phenotypes.

Variant displays