Product Details
- SNP ID
-
rs146406246
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.8:23137949 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GGAGCCCACCAGTTGGTCCTGAATT[A/G]TTTCCTTTGCATGTCCTTCTTCCAG
- Phenotype
-
MIM: 603614
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
TNFRSF10D
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs544173189,rs562492349] 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
- TNFRSF10D
- Gene Name
- TNF receptor superfamily member 10d
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_003840.4 |
1177 |
Missense Mutation |
ACA,ATA |
T361I |
NP_003831.2 |
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