Original source

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

C/G | Ancestral: C | Ambiguity code: S

Chromosome 4:73853907 (forward strand) | View in location tab


with COSMIC COSM1633775 (C/G)

Most severe consequence
Splice region variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 37 sample genotypes.

Variant displays