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AGTGAAGCGCTTAGAAATGCAAGAC[A/G]TGTTGTGAAGCACGATGCCGAGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616512 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF152 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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RNF152 - ring finger protein 152 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173557.2 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | NP_775828.1 | |
XM_005266650.3 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_005266707.1 | |
XM_005266652.3 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_005266709.1 | |
XM_011525878.2 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_011524180.1 | |
XM_011525879.2 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_011524181.1 | |
XM_017025612.1 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_016881101.1 | |
XM_017025613.1 | 1182 | Missense Mutation | ACG,ATG | T,M 190 | XP_016881102.1 |