Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 4:38797171 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM114630

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB NM_003263.3:c.1661A>G

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and is associated with 1 phenotype.

Variant displays