Product Details
- SNP ID
-
rs146717788
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:100487756 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCAAAGCTTCCTGCATCCACACATC[A/G]GGCAACCTCATGGAGCCCAGCCACG
- Phenotype
-
MIM: 610258
MIM: 601396
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
SEC31B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2298074] 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
- SEC31B
- Gene Name
- SEC31 homolog B, COPII coat complex component
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_015490.3 |
3502 |
Nonsense Mutation |
CGA,TGA |
R1134* |
NP_056305.1 |
- Gene
- WNT8B
- Gene Name
- Wnt family member 8B
There are no transcripts associated with this gene.
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