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CAGCTGACGTCTTCTCCAGCTCTGC[A/G]ATGCGTGTCTGCTGCTGCTGTACCA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
RNF41 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)
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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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RNF41 - ring finger protein 41 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242826.1 | 878 | Silent Mutation | ATC,ATT | I,I 149 | NP_001229755.1 | |
NM_005785.3 | 878 | Silent Mutation | ATC,ATT | I,I 149 | NP_005776.1 | |
NM_194358.2 | 878 | Silent Mutation | ATC,ATT | I,I 78 | NP_919339.1 | |
NM_194359.2 | 878 | Silent Mutation | ATC,ATT | I,I 149 | NP_919340.1 | |
XM_005268561.4 | 878 | Silent Mutation | ATC,ATT | I,I 78 | XP_005268618.1 | |
XM_011537734.2 | 878 | Silent Mutation | ATC,ATT | I,I 78 | XP_011536036.1 | |
XM_011537735.2 | 878 | Silent Mutation | ATC,ATT | I,I 78 | XP_011536037.1 |