Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGGGGCCCGCCCTCAAGATCCGGG[C/T]CCAGGTGAGACGCTGGGGAGTGAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
3 submissions
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Phenotype: |
MIM: 610770 MIM: 616765 | ||||||||||||||||||||
Literature Links: |
NOC2L PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
NOC2L - NOC2 like nucleolar associated transcriptional repressor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015658.3 | 1876 | Intron | NP_056473.2 |
SAMD11 - sterile alpha motif domain containing 11 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152486.2 | 1876 | Missense Mutation | GCC,GTC | A,V 599 | NP_689699.2 |