Product Details
- SNP ID
-
rs28412031
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:23320610 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CCAGTCTGTTAGCGGTGCAGATTGG[A/G]GGGGTGACATTGGAAGCTGTCCAGG
- Phenotype
-
MIM: 601931
MIM: 602279
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
BCL2L2
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs140736009] 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
- BCL2L2
- Gene Name
- BCL2 like 2
There are no transcripts associated with this gene.
- Gene
- BCL2L2-PABPN1
- Gene Name
- BCL2L2-PABPN1 readthrough
- Gene
- PABPN1
- Gene Name
- poly(A) binding protein nuclear 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_004643.3 |
423 |
UTR 5 |
|
|
NP_004634.1 |
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