Product Details
- SNP ID
-
rs35077427
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.22:19848233 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- AAATAAAATCTCTGGGTATTTCCAA[A/G]GGAAGTGAAGGACTGACACCATGAT
- Phenotype
-
MIM: 610778
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
C22orf29
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs75749250] 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
- C22orf29
- Gene Name
- chromosome 22 open reading frame 29
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_024627.5 |
4540 |
UTR 3 |
|
|
NP_078903.3 |
- Gene
- GNB1L
- Gene Name
- G protein subunit beta 1 like
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_053004.2 |
4540 |
Intron |
|
|
NP_443730.1 |
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