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CGGCCCGCCCGGCGGGGCGGCAGAG[A/C]TGCTGCTCTGGCTCCCAAGCCGCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614148 MIM: 602241 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C1QTNF9B 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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C1QTNF9B - C1q and tumor necrosis factor related protein 9B | ||||||
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There are no transcripts associated with this gene. |
C1QTNF9B-AS1 - C1QTNF9B antisense RNA 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014442.2 | 174 | Intron | NP_001014442.2 | |||
NM_001135816.1 | 174 | Intron | NP_001129288.1 |
MIPEP - mitochondrial intermediate peptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005932.3 | 174 | Missense Mutation | GCT,TCT | A,S 16 | NP_005923.2 | |
XM_011535097.2 | 174 | Intron | XP_011533399.1 | |||
XM_011535098.2 | 174 | Missense Mutation | GCT,TCT | A,S 16 | XP_011533400.1 |