Original source

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

Alleles
T/C|Ancestral: T|Ambiguity code: Y
Location

Chromosome 16:88648088 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

HGVS names

This variant has 18 HGVS names - Show

About this variant

This variant overlaps 16 transcripts and is mentioned in 1 citation.

Variant displays