IL18BP
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604113
MIM: 164009
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Literature Links: |
IL18BP PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| IL18BP - interleukin 18 binding protein | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001039659.1 | 1511 | Intron | NP_001034748.1 | |||
| NM_001039660.1 | 1511 | Intron | NP_001034749.1 | |||
| NM_001145055.1 | 1511 | Intron | NP_001138527.1 | |||
| NM_001145057.1 | 1511 | Intron | NP_001138529.1 | |||
| NM_005699.3 | 1511 | Missense Mutation | AGC,TGC | S,C 197 | NP_005690.2 | |
| NM_173042.2 | 1511 | Intron | NP_766630.2 | |||
| NM_173044.2 | 1511 | Intron | NP_766632.2 | |||
| XM_017017059.1 | 1511 | Intron | XP_016872548.1 | |||
| XM_017017060.1 | 1511 | Intron | XP_016872549.1 | |||
| XM_017017061.1 | 1511 | Intron | XP_016872550.1 | |||
| XM_017017062.1 | 1511 | Intron | XP_016872551.1 | |||
| XM_017017063.1 | 1511 | Intron | XP_016872552.1 | |||
| NUMA1 - nuclear mitotic apparatus protein 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| RNF121 - ring finger protein 121 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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