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AGGTTAGGGAGGGGGCGACGCTGAG[A/G]TGGGGGCGGCGGCGGCGGAAGCGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612413 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C11orf71 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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C11orf71 - chromosome 11 open reading frame 71 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271562.1 | 144 | Intron | NP_001258491.1 | |||
NM_019021.3 | 144 | Intron | NP_061894.2 |
RBM7 - RNA binding motif protein 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286045.1 | 144 | Missense Mutation | ATG,GTG | M,V 1 | NP_001272974.1 | |
NM_001286046.1 | 144 | UTR 5 | NP_001272975.1 | |||
NM_001286047.1 | 144 | UTR 5 | NP_001272976.1 | |||
NM_001286048.1 | 144 | UTR 5 | NP_001272977.1 | |||
NM_016090.3 | 144 | Missense Mutation | ATG,GTG | M,V 1 | NP_057174.1 |