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 17:50201450 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM062525

Most severe consequence
 
Missense variant
Evidence status

Synonyms
HGVS names

This variant has 14 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and 2 regulatory features.

Variant displays