Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 15 HGVS names - click the plus to show

Variation displays