Product Details

SNP ID

rs143621551

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.20:18024930 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCTGGGTGAAGGCTTTATTGCAGAC[A/G]TTGCATTTGTAGGGACGAATGCCTG

Phenotype

MIM: 616441

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

OVOL2 PubMed Links

Additional Information

For this assay, SNP(s) [rs2281543] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

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	782	Silent Mutation	AAC,AAT	N46N	NP_001290390.1
NM_001303462.1	782	Silent Mutation	AAC,AAT	N46N	NP_001290391.1
NM_021220.3	782	Silent Mutation	AAC,AAT	N178N	NP_067043.2

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