Product Details
- SNP ID
-
rs145791963
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:127850609 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACTAACCTTGGGATTAGAGCCTTGG[A/C]CTCCTCAGCAGTCTCTGGGCAAAGG
- Phenotype
-
MIM: 606017
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
LOC107985803
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs11556864] 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
- LOC107985803
- Gene Name
- uncharacterized LOC107985803
There are no transcripts associated with this gene.
- Gene
- POLR2D
- Gene Name
- RNA polymerase II subunit D
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004805.3 |
386 |
Missense Mutation |
GCC,TCC |
A111S |
NP_004796.1 |
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