Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

Chromosome 10:49625634 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM014853

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 1 sample genotype and is associated with 2 phenotypes.

Variant displays