Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome 9:95101742 (forward strand) | View in location tab


with COSMIC COSM1206492 (G/A) ; HGMD-PUBLIC CM930241 ; PhenCode FANCC:c.1642C>T (G/A)

Most severe consequence
Evidence status

Clinical significance


LSDB 6273, NM_000136.2:c.1642C>T_1265076212

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 4 transcripts and is associated with 3 phenotypes.

Variation displays