Product Details
- SNP ID
-
hCV104005334
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:112090211 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TATAATTCAGAGTTGTGGGTGGTCT[A/G]TTTTTATTCTTGCTTGCACACCGCC
- Phenotype
-
MIM: 607345
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FAM229B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs111830279] are located under a probe 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
- FAM229B
- Gene Name
- family with sequence similarity 229 member B
There are no transcripts associated with this gene.
- Gene
- TUBE1
- Gene Name
- tubulin epsilon 1
There are no transcripts associated with this gene.
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