Product Details

SNP ID
rs200097484
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.20:18024824 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTGTAGCCGCAATCCTCGCAGACGT[A/G]GAGCTTGTCCCGCCGCTGCTTATAG
Phenotype
MIM: 616441
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
OVOL2 PubMed Links

Gene Details

Gene
OVOL2
Gene Name
ovo like zinc finger 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001303461.1 888 Missense Mutation CAC,TAC H82Y NP_001290390.1
NM_001303462.1 888 Missense Mutation CAC,TAC H82Y NP_001290391.1
NM_021220.3 888 Missense Mutation CAC,TAC H214Y NP_067043.2

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