Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
42 submissions
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Phenotype: |
MIM: 191191 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
MIR4632 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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MIR4632 - microRNA 4632 | ||||||
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There are no transcripts associated with this gene. |
TNFRSF1B - TNF receptor superfamily member 1B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001066.2 | 835 | Missense Mutation | CCG,CTG | P,L 264 | NP_001057.1 | |
XM_011542060.2 | 835 | Missense Mutation | CCG,CTG | P,L 264 | XP_011540362.1 | |
XM_011542063.2 | 835 | Missense Mutation | CCG,CTG | P,L 264 | XP_011540365.1 | |
XM_017002211.1 | 835 | Missense Mutation | CCG,CTG | P,L 264 | XP_016857700.1 | |
XM_017002212.1 | 835 | Missense Mutation | CCG,CTG | P,L 213 | XP_016857701.1 | |
XM_017002213.1 | 835 | Missense Mutation | CCG,CTG | P,L 213 | XP_016857702.1 | |
XM_017002214.1 | 835 | Missense Mutation | CCG,CTG | P,L 69 | XP_016857703.1 | |
XM_017002215.1 | 835 | Missense Mutation | CCG,CTG | P,L 69 | XP_016857704.1 |
Set Membership: |
HapMap |