Product Details
- SNP ID
-
rs2977677
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:91955344 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CACTTTGAAGAGAAAATAAGATGCA[G/T]TAACACATTAAAAATAGGCAACTTG
- Phenotype
-
MIM: 133435
- Polymorphism
- G/T, Transversion substitution
- Allele Nomenclature
-
- Literature Links
-
RUNX1T1
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77807575] 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
- RUNX1T1
- Gene Name
- RUNX1 translocation partner 1
View Full Product Details