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- SNP ID:
- rs143853699
- Gene
-
NOC2LSAMD11 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 944531 - 944531 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
ACCAGCCCAGCCCAGCCCAGCTCTC[A/G]ATACGTTTGGTCTTTCATGCTGAAA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 submissions
|
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Phenotype: |
MIM: 610770
MIM: 616765
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Literature Links: |
NOC2L PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| NOC2L - NOC2 like nucleolar associated transcriptional repressor | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_015658.3 | 2504 | Intron | NP_056473.2 | |||
| SAMD11 - sterile alpha motif domain containing 11 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_152486.2 | 2504 | UTR 3 | NP_689699.2 | |||
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