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 16:23380731 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM951144, CM050080, CM056053

Most severe consequence
 
Missense variant
Synonyms

LSDB 9509, 9503

This variant has 20 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts.

Variant displays