Original source

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

C/A|Ancestral: C|Ambiguity code: M

Chromosome 14:35404550 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM033654 ; PhenCode NFKBIAbase_D0063:g.1189G>T (C/A)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 11 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays