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AGCAAGACTTTTAACAAGATGCCTC[C/T]TCAAAGGGGCGGCGGCAGCAGCAAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615998 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF10 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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RNF10 - ring finger protein 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014868.4 | 793 | Missense Mutation | CCT,CTT | P,L 97 | NP_055683.3 | |
XM_005254013.2 | 793 | Missense Mutation | CCT,CTT | P,L 47 | XP_005254070.1 | |
XM_006719717.2 | 793 | Missense Mutation | CCT,CTT | P,L 97 | XP_006719780.1 | |
XM_017020282.1 | 793 | Missense Mutation | CCT,CTT | P,L 47 | XP_016875771.1 | |
XM_017020283.1 | 793 | Missense Mutation | CCT,CTT | P,L 97 | XP_016875772.1 |