Product Details
- SNP ID
-
rs144383122
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:16939601 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCACACACACAATGCCAAGGCCACT[C/G]TCTGGGATGTGTGGGCAAGGCTGCA
- Phenotype
-
MIM: 604907
- Polymorphism
- C/G, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
TNFRSF13B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs11078355] 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
- TNFRSF13B
- Gene Name
- TNF receptor superfamily member 13B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_012452.2 |
841 |
Missense Mutation |
GAC,GAG |
D276E |
NP_036584.1 |
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