Product Details
- SNP ID
-
rs201806315
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:49132142 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CACAGTCTGCACGTGCGTGTAGAAG[A/G]CACACACACTCTGCGGAGCAGCATT
- Phenotype
-
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
FAM170B
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs41280539] 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
- FAM170B
- Gene Name
- family with sequence similarity 170 member B
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001164484.1 |
425 |
Missense Mutation |
GCC,GTC |
A108V |
NP_001157956.1 |
- Gene
- FAM170B-AS1
- Gene Name
- FAM170B antisense RNA 1
There are no transcripts associated with this gene.
- Gene
- VSTM4
- Gene Name
- V-set and transmembrane domain containing 4
There are no transcripts associated with this gene.
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