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AGGACCTCTCTGCGGCCACGTCCTA[C/T]ACCGAAGATGATTTCTACTGCCCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610432 MIM: 616319 | ||||||||||||||||||||
Literature Links: |
RNF125 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 |
RNF125 - ring finger protein 125 | ||||||
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There are no transcripts associated with this gene. |
RNF138 - ring finger protein 138 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001191324.1 | 491 | Silent Mutation | TAC,TAT | Y,Y 11 | NP_001178253.2 | |
NM_016271.4 | 491 | Silent Mutation | TAC,TAT | Y,Y 11 | NP_057355.2 | |
NM_198128.2 | 491 | Silent Mutation | TAC,TAT | Y,Y 11 | NP_937761.1 | |
XM_005258285.1 | 491 | Intron | XP_005258342.1 | |||
XM_005258286.1 | 491 | Silent Mutation | TAC,TAT | Y,Y 11 | XP_005258343.1 |