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GAAGCACCCTCTGGCCAGGGACACC[C/G]CAGTCTGCCTCCTCGCTGTCCTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601237 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF112 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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RNF112 - ring finger protein 112 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007148.4 | 474 | Missense Mutation | CCA,GCA | P,A 168 | NP_009079.2 | |
XM_006721571.3 | 474 | Missense Mutation | CCA,GCA | P,A 168 | XP_006721634.1 | |
XM_006721572.3 | 474 | Missense Mutation | CCA,GCA | P,A 167 | XP_006721635.1 | |
XM_006721573.3 | 474 | Missense Mutation | CCA,GCA | P,A 144 | XP_006721636.1 |