Product Details
- SNP ID
-
rs137922914
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.11:8937822 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- TCTGGCAGATGATGGCGGAGCTGGG[A/C]GTAGCCTTCATTGACACATTTCACC
- Phenotype
-
MIM: 609154
- Polymorphism
- A/C, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
ASCL3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs2742505] 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
- ASCL3
- Gene Name
- achaete-scute family bHLH transcription factor 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_020646.2 |
400 |
Missense Mutation |
|
|
NP_065697.1 |
- Gene
- C11orf16
- Gene Name
- chromosome 11 open reading frame 16
There are no transcripts associated with this gene.
- Gene
- TMEM9B
- Gene Name
- TMEM9 domain family member B
There are no transcripts associated with this gene.
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