Original source

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

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

Chromosome 4:73419634 (forward strand) | View in location tab


with COSMIC COSM109220 (G/A) ; HGMD-PUBLIC CM910027

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB AlbB,Oliphant, NC_000004.10:g.74504215G>A

This variant has 21 HGVS names - click the plus to show

About this variant

This variant overlaps 15 transcripts, is associated with 3 phenotypes and is mentioned in 3 citations.

Somatic mutation displays