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GTCTCTGCCAGAAGAGGTGTGGCAT[C/T]CCCCAAGGGGCCTTGGCCCTCAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605350 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL27RA 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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IL27RA - interleukin 27 receptor subunit alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004843.3 | 1810 | Intron | NP_004834.1 |
PALM3 - paralemmin 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145028.1 | 1810 | Missense Mutation | AAT,GAT | N,D 604 | NP_001138500.1 | |
XM_005259891.4 | 1810 | Missense Mutation | AAT,GAT | N,D 619 | XP_005259948.1 | |
XM_011527965.2 | 1810 | Missense Mutation | AAT,GAT | N,D 592 | XP_011526267.1 |