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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_058460

HGVS names

This variant has 22 HGVS names - Show

About this variant

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

Variant displays