Product Details
- SNP ID
-
rs10107826
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:23103141 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- CATACCATGGCCCGGATCCCCAAGA[C/T]CCTAAAGTTCGTCGTCGTCATCGTC
- Phenotype
-
MIM: 603613
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
LOC254896
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs10107827] 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
- LOC254896
- Gene Name
- uncharacterized LOC254896
There are no transcripts associated with this gene.
- Gene
- TNFRSF10C
- Gene Name
- TNF receptor superfamily member 10c
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003841.3 |
328 |
Missense Mutation |
ACC,ATC |
T7I |
NP_003832.2 |
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