Product Details
- SNP ID
-
rs16828077
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.2:231455699 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GTCCCAAGTTAACTGTACATGCTGG[A/G]GAGCCATCCCACAGAAAGTAGCCTT
- Phenotype
-
MIM: 164035
MIM: 604012
MIM: 611133
- Polymorphism
- A/G, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
NCL
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs77122043] 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
- NCL
- Gene Name
- nucleolin
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_005381.2 |
|
Intron |
|
|
NP_005372.2 |
- Gene
- SNORA75
- Gene Name
- small nucleolar RNA, H/ACA box 75
There are no transcripts associated with this gene.
- Gene
- SNORD20
- Gene Name
- small nucleolar RNA, C/D box 20
There are no transcripts associated with this gene.
- Gene
- SNORD82
- Gene Name
- small nucleolar RNA, C/D box 82
There are no transcripts associated with this gene.
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