Unique variants in gene OR2D3

Information The variants shown are described using the NM_001004684.1 transcript reference sequence.

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Effect     

Reported     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-?/. 1 - c.896_898dup r.(?) p.(Pro299_Met300insThr) - likely benign g.6943128_6943130dup g.6921897_6921899dup OR2D3(NM_001004684.1):c.895_896insCAA (p.(Pro299_Met300insThr)) - OR2D3_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
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