Product Details

SNP ID

rs28635799

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.4:80327890 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGAAGTTTAGCCAAGGTGGTGGAAT[A/T]AAAAAGTTACACTAATAAGAACAGG

Phenotype

Polymorphism

A/T, Transversion Substitution

Allele Nomenclature

Literature Links

C4orf22 PubMed Links

Additional Information

For this assay, SNP(s) [rs76828977] 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

C4orf22

Gene Name

chromosome 4 open reading frame 22

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001206997.1		Intron			NP_001193926.1
NM_152770.2		Intron			NP_689983.2
XM_011531816.2		Intron			XP_011530118.2
XM_017007972.1		Intron			XP_016863461.1
XM_017007973.1		Intron			XP_016863462.1
XM_017007974.1		Intron			XP_016863463.1
XM_017007975.1		Intron			XP_016863464.1
XM_017007976.1		Intron			XP_016863465.1
XM_017007977.1		Intron			XP_016863466.1
XM_017007978.1		Intron			XP_016863467.1

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