Original source

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

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

Chromosome 16:88810141 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM940079

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_010_APRT_102600_0007

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and is associated with 2 phenotypes.

Variant displays