Original source

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

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

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

Co-located

with COSMIC COSM1633775 (C/G)

Most severe consequence
 
Splice region variant
Evidence status

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts and has 37 sample genotypes.

Variant displays