Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCGTCGCCGTCTGGGCCGCGCTG[A/G]CCGTCGGACTGGAGCTCTGGGCTGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 191191 | ||||||||||||||||||||
Literature Links: |
MIR7846 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MIR7846 - microRNA 7846 | ||||||
---|---|---|---|---|---|---|
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 | 175 | Missense Mutation | ACC,GCC | T,A 11 | NP_001057.1 | |
XM_011542060.2 | 175 | Missense Mutation | ACC,GCC | T,A 11 | XP_011540362.1 | |
XM_011542063.2 | 175 | Missense Mutation | ACC,GCC | T,A 11 | XP_011540365.1 | |
XM_017002211.1 | 175 | Missense Mutation | ACC,GCC | T,A 11 | XP_016857700.1 | |
XM_017002212.1 | 175 | Intron | XP_016857701.1 | |||
XM_017002213.1 | 175 | Intron | XP_016857702.1 | |||
XM_017002214.1 | 175 | UTR 5 | XP_016857703.1 | |||
XM_017002215.1 | 175 | UTR 5 | XP_016857704.1 |