Product Details

SNP ID
rs314262
Assay Type
Validated
NCBI dbSNP Submissions
NA
Location
Chr.6:104946746 on Build GRCh38
Set Membership
HapMap Validated
Context Sequence [VIC/FAM]
TGCTTTCCAAAGAATGTAGTTCAGT[A/G]ATAGTTGACACATACTATAGATTAA
Phenotype
MIM: 611044
Polymorphism
A/G, Transition Substitution
Allele Nomenclature
Literature Links
LIN28B PubMed Links
Additional Information
For this assay, SNP(s) [rs73771026] 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
LIN28B
Gene Name
lin-28 homolog B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001004317.3 Intron NP_001004317.1
XM_006715477.2 Intron XP_006715540.2
XM_011535818.2 Intron XP_011534120.1
Gene
LIN28B-AS1
Gene Name
LIN28B antisense RNA 1
There are no transcripts associated with this gene.

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