Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 14:104769796 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 19 transcripts.

Variant displays