Product Details

SNP ID
rs7327634
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.13:52013609 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTTCCCACCTAAATTATTTGAAGGA[A/C]TTGCCAGAAAAACCTTTACATTATA
Phenotype
MIM: 613666 MIM: 606882
Polymorphism
A/C, Transversion Substitution
Allele Nomenclature
Literature Links
ALG11 PubMed Links
Additional Information
For this assay, SNP(s) [rs7328090] 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
ALG11
Gene Name
ALG11, alpha-1,2-mannosyltransferase
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004127.2 Intron NP_001004127.2
Gene
ATP7B
Gene Name
ATPase copper transporting beta
There are no transcripts associated with this gene.

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