Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome 12:40321114 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM043519

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

12:g.40321114A>G
ENST00000479187.3:n.1777A>G
ENST00000298910.9:c.5096A>G
ENSP00000298910.7:p.Tyr1699Cys
ENST00000430804.3:c.*1769A>G

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays