Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGACGTCTTCTCCAGCTCTGCGATG[C/T]GTGTCTGCTGCTGCTGTACCACTGA
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 - 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 |
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 | 874 | Missense Mutation | CAC,CGC | H,R 148 | NP_001229755.1 | |
NM_005785.3 | 874 | Missense Mutation | CAC,CGC | H,R 148 | NP_005776.1 | |
NM_194358.2 | 874 | Missense Mutation | CAC,CGC | H,R 77 | NP_919339.1 | |
NM_194359.2 | 874 | Missense Mutation | CAC,CGC | H,R 148 | NP_919340.1 | |
XM_005268561.4 | 874 | Missense Mutation | CAC,CGC | H,R 77 | XP_005268618.1 | |
XM_011537734.2 | 874 | Missense Mutation | CAC,CGC | H,R 77 | XP_011536036.1 | |
XM_011537735.2 | 874 | Missense Mutation | CAC,CGC | H,R 77 | XP_011536037.1 |