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ACATTTCTGAGTCCGCATACATCCC[A/G]TTGATTAAGTAGTCCACCTGGGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610880 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C11orf24 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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C11orf24 - chromosome 11 open reading frame 24 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001300913.1 | 1765 | Silent Mutation | AAC,AAT | N,N 106 | NP_001287842.1 | |
NM_022338.3 | 1765 | Silent Mutation | AAC,AAT | N,N 441 | NP_071733.1 | |
XM_005274053.3 | 1765 | Silent Mutation | AAC,AAT | N,N 441 | XP_005274110.1 | |
XM_011545103.2 | 1765 | Silent Mutation | AAC,AAT | N,N 409 | XP_011543405.1 |