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CAGCTGGTGTTTGTGTTCAGCTGAC[A/G]TCTTCTCCAGCTCTGCGATGCGTGT
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) - 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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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 | 895 | Missense Mutation | ACG,ATG | T,M 155 | NP_001229755.1 | |
NM_005785.3 | 895 | Missense Mutation | ACG,ATG | T,M 155 | NP_005776.1 | |
NM_194358.2 | 895 | Missense Mutation | ACG,ATG | T,M 84 | NP_919339.1 | |
NM_194359.2 | 895 | Missense Mutation | ACG,ATG | T,M 155 | NP_919340.1 | |
XM_005268561.4 | 895 | Missense Mutation | ACG,ATG | T,M 84 | XP_005268618.1 | |
XM_011537734.2 | 895 | Missense Mutation | ACG,ATG | T,M 84 | XP_011536036.1 | |
XM_011537735.2 | 895 | Missense Mutation | ACG,ATG | T,M 84 | XP_011536037.1 |