Original source

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

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

Chromosome 1:16990213 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_058460

This variant has 22 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and is mentioned in 1 citation.

Variant displays