Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.05 (A)

Chromosome 9:35076758 (forward strand) | View in location tab


with COSMIC COSM150601 (G/A) ; HGMD-PUBLIC CM015016 ; PhenCode FANCG:c.890C>T (G/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 4148 sample genotypes and is associated with 1 phenotype.

Variant displays