Original source

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

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

Chromosome 14:24259950 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM013051

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 5807

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature and is associated with 2 phenotypes.

Variant displays