Product Details

SNP ID

rs1984388

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:31938035 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CATGGTCCAAAGACTTGTCTTTTGA[A/T]GCAGCCCTGTTGTATCCTCTTGAGT

Phenotype

MIM: 113508

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

C22orf24 PubMed Links

Additional Information

For this assay, SNP(s) [rs75883264] 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

C22orf24

Gene Name

chromosome 22 open reading frame 24

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001302819.1	211	Missense Mutation	CAT,CTT	H78L	NP_001289748.1
NM_001302820.1	211	Missense Mutation	CAT,CTT	H78L	NP_001289749.1
NM_015372.2	211	Missense Mutation	CAT,CTT	H11L	NP_056187.1

Gene

YWHAH

Gene Name

tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein eta

There are no transcripts associated with this gene.

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