Product Details

SNP ID

rs4820891

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.22:30636322 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CAGGCCTGGCACAAGTAAGCAGTGT[C/T]CTCACCTGTCTGAAACGGGACACGG

Phenotype

MIM: 613441

Polymorphism

C/T, Transition Substitution

Allele Nomenclature

Literature Links

SLC35E4 PubMed Links

Additional Information

For this assay, SNP(s) [rs7289904] 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

SLC35E4

Gene Name

solute carrier family 35 member E4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001479.3	1600	UTR 5			NP_001001479.1
NM_001318370.1	1600	UTR 5			NP_001305299.1
NM_001318371.1	1600	UTR 5			NP_001305300.1
XM_017028794.1	1600	UTR 5			XP_016884283.1
XM_017028795.1	1600	UTR 5			XP_016884284.1

Gene

TCN2

Gene Name

transcobalamin 2

There are no transcripts associated with this gene.

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