Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

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

Co-located variants

HGMD-PUBLIC CM110093, CM085952

Most severe consequence
Missense variant

This variant has 3 synonyms - Show

HGVS names

This variant has 42 HGVS names - Show

About this variant

This variant overlaps 36 transcripts and 1 regulatory feature.

Variant displays