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CTGACTGCCCACTATGACTGTGGCA[A/G]GCAGAAGGCTGACTGTAAAGAGAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 179616 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C11orf74 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C11orf74 - chromosome 11 open reading frame 74 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001276722.1 | 69 | Intron | NP_001263651.1 | |||
NM_001276723.1 | 69 | Intron | NP_001263652.1 | |||
NM_001276724.1 | 69 | Intron | NP_001263653.1 | |||
NM_001276725.1 | 69 | Intron | NP_001263654.1 | |||
NM_001276726.1 | 69 | Intron | NP_001263655.1 | |||
NM_001276727.1 | 69 | Intron | NP_001263656.1 | |||
NM_138787.3 | 69 | Intron | NP_620142.2 | |||
XM_006718138.3 | 69 | Intron | XP_006718201.1 | |||
XM_011519885.2 | 69 | Intron | XP_011518187.1 |
RAG2 - recombination activating gene 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000536.3 | 69 | UTR 5 | NP_000527.2 | |||
NM_001243785.1 | 69 | UTR 5 | NP_001230714.1 | |||
NM_001243786.1 | 69 | UTR 5 | NP_001230715.1 |