Product Details

SNP ID
rs1055314
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.21:34791995 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGGCCTGACCTACAGCGAGATCCTG[G/T]CCGTCGGGCGCCCTCGGCCCCAGGA
Phenotype
MIM: 151385
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
LINC01426 PubMed Links
Additional Information
For this assay, SNP(s) [rs539980908] 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
LINC01426
Gene Name
long intergenic non-protein coding RNA 1426
There are no transcripts associated with this gene.

Gene
RUNX1
Gene Name
runt related transcription factor 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001001890.2 1578 UTR 3 NP_001001890.1
NM_001122607.1 1578 Intron NP_001116079.1
NM_001754.4 1578 UTR 3 NP_001745.2
XM_005261068.3 1578 UTR 3 XP_005261125.1
XM_005261069.4 1578 UTR 3 XP_005261126.1
XM_011529766.2 1578 UTR 3 XP_011528068.1
XM_011529767.2 1578 UTR 3 XP_011528069.1
XM_011529768.2 1578 UTR 3 XP_011528070.1
XM_011529770.2 1578 Intron XP_011528072.1
XM_017028487.1 1578 UTR 3 XP_016883976.1

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