Product Details
- SNP ID
-
rs148183380
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:127701618 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCGCGGAGCCGCTGCTCGCCGCGGA[G/T]AAGGCGGAGGAGCCCGGGGACCGGC
- Phenotype
-
- Polymorphism
- G/T, Transversion Substitution
- Allele Nomenclature
-
- Literature Links
-
SFT2D3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs141206501] 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
- SFT2D3
- Gene Name
- SFT2 domain containing 3
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_032740.3 |
596 |
Missense Mutation |
GAG,GAT |
E30D |
NP_116129.3 |
- Gene
- WDR33
- Gene Name
- WD repeat domain 33
There are no transcripts associated with this gene.
View Full Product Details