Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CATCCAGCCTCACTTGCCTGCCGAT[A/G]AGGCCCGGGGTACACAGGGCCCCGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
11 submissions
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Phenotype: |
MIM: 191191 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TNFRSF1B 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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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 | 963 | Missense Mutation | AAG,GAG | K,E 307 | NP_001057.1 | |
XM_011542060.2 | 963 | Missense Mutation | AAG,GAG | K,E 307 | XP_011540362.1 | |
XM_011542063.2 | 963 | Missense Mutation | AAG,GAG | K,E 307 | XP_011540365.1 | |
XM_017002211.1 | 963 | Intron | XP_016857700.1 | |||
XM_017002212.1 | 963 | Intron | XP_016857701.1 | |||
XM_017002213.1 | 963 | Intron | XP_016857702.1 | |||
XM_017002214.1 | 963 | Missense Mutation | AAG,GAG | K,E 112 | XP_016857703.1 | |
XM_017002215.1 | 963 | Missense Mutation | AAG,GAG | K,E 112 | XP_016857704.1 |