Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V
Location

Chromosome 6:10404512 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM085952, CM110093

Most severe consequence
 
Missense variant

This variant has 3 synonyms - click the plus to show

This variant has 42 HGVS names - click the plus to show

About this variant

This variant overlaps 36 transcripts and 1 regulatory feature.

Variant displays