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CGCTGGCTGTGGTGGTGGCAATGCG[C/T]GGAGAACGGCGGGTTCCACTGCGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604113 MIM: 164009 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL18BP 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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IL18BP - interleukin 18 binding protein | ||||||
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There are no transcripts associated with this gene. |
NUMA1 - nuclear mitotic apparatus protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001286561.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2074 | NP_001273490.1 | |
NM_006185.3 | 6469 | Silent Mutation | CCA,CCG | P,P 2088 | NP_006176.2 | |
XM_006718564.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2088 | XP_006718627.1 | |
XM_011545054.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543356.1 | |
XM_011545055.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543357.1 | |
XM_011545056.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543358.1 | |
XM_011545057.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543359.1 | |
XM_011545058.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543360.1 | |
XM_011545059.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543361.1 | |
XM_011545060.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543362.1 | |
XM_011545061.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543363.1 | |
XM_011545062.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543364.1 | |
XM_011545063.2 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543365.1 | |
XM_011545064.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2106 | XP_011543366.1 | |
XM_011545065.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2092 | XP_011543367.1 | |
XM_011545066.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2074 | XP_011543368.1 | |
XM_017017830.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2074 | XP_016873319.1 | |
XM_017017831.1 | 6469 | Silent Mutation | CCA,CCG | P,P 2074 | XP_016873320.1 |
RNF121 - ring finger protein 121 | ||||||
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There are no transcripts associated with this gene. |