Product Details
- SNP ID
-
rs2959615
- Assay Type
- Validated
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:17248189 on Build GRCh38
- Set Membership
-
HapMap
Validated
- Context Sequence [VIC/FAM]
- ACTGCTTCTTTATATTTTATGCATT[C/T]TGCAAGTATATTTACTTAACAGTTT
- Phenotype
-
MIM: 604913
MIM: 609927
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
CNOT7
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs201492160] 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
- CNOT7
- Gene Name
- CCR4-NOT transcription complex subunit 7
There are no transcripts associated with this gene.
- Gene
- VPS37A
- Gene Name
- VPS37A, ESCRT-I subunit
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