Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B
Location

Chromosome 16:31191418 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM091086, CM104702, CM091090

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 28 HGVS names - click the plus to show

About this variant

This variant overlaps 26 transcripts and is associated with 4 phenotypes.

Variant displays