Original source

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

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

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

Co-located variants

HGMD-PUBLIC CM951144, CM056053, CM050080

Most severe consequence
 
Missense variant
Synonyms

LSDB 9509, 9503

HGVS names

This variant has 20 HGVS names - Show

About this variant

This variant overlaps 10 transcripts.

Variant displays