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CTGGTTCCCTTGGGCTCCGGCCGCC[A/C]CCATCCACTCGACGGCTCTCGGCCC
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 |
---|---|---|
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 |
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 | 429 | Silent Mutation | GGG,GGT | G,G 70 | NP_001258491.1 | |
NM_019021.3 | 429 | Silent Mutation | GGG,GGT | G,G 70 | 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 | 429 | Intron | NP_001272974.1 | |||
NM_001286046.1 | 429 | Intron | NP_001272975.1 | |||
NM_001286047.1 | 429 | Intron | NP_001272976.1 | |||
NM_001286048.1 | 429 | Intron | NP_001272977.1 | |||
NM_016090.3 | 429 | Intron | NP_057174.1 |