Original source

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

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

Chromosome 11:34966740 (forward strand) | View in location tab


with HGMD-PUBLIC CM042447

Most severe consequence
Stop gained
Evidence status

Clinical significance

This variant has 2 synonyms - click the plus to show

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 1 sample genotype and is associated with 2 phenotypes.

Variant displays