Original source

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

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

Chromosome 4:148152550 (forward strand) | View in location tab


with COSMIC COSM420178 (G/A) ; HGMD-PUBLIC CM001739

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, has 2 individual genotypes and is associated with 3 phenotypes.

Variation displays