Original source

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

Alleles
C/G/T | Ancestral: C | Ambiguity code: B | MAF: < 0.01 (T)
Location

Chromosome 17:39471420 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_041968

This variant has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 8 transcripts and has 2504 sample genotypes.

Variant displays