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GGCTTAAGCTCCAGCGGTTGTTGCA[A/G]TTCATCCACCTGTCTGGATACCCAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605580 MIM: 600556 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL23A 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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IL23A - interleukin 23 subunit alpha | ||||||
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There are no transcripts associated with this gene. |
STAT2 - signal transducer and activator of transcription 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005419.3 | 1649 | Silent Mutation | CTG,TTG | L,L 706 | NP_005410.1 | |
NM_198332.1 | 1649 | Silent Mutation | CTG,TTG | L,L 702 | NP_938146.1 | |
XM_005269111.3 | 1649 | Intron | XP_005269168.2 | |||
XM_011538697.2 | 1649 | Silent Mutation | CTG,TTG | L,L 714 | XP_011536999.1 | |
XM_011538698.2 | 1649 | Silent Mutation | CTG,TTG | L,L 710 | XP_011537000.1 | |
XM_011538699.2 | 1649 | Intron | XP_011537001.1 | |||
XM_011538700.2 | 1649 | Silent Mutation | CTG,TTG | L,L 470 | XP_011537002.1 | |
XM_017019904.1 | 1649 | Silent Mutation | CTG,TTG | L,L 462 | XP_016875393.1 |