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AATGGATTTGTACAACCAACCCGAG[C/G]CTGTGAAGTCCTTTCTCTTCTACCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605509 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL36A 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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IL36A - interleukin 36, alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014440.2 | 712 | Missense Mutation | CCT,GCT | P,A 101 | NP_055255.1 | |
XM_005263639.2 | 712 | Missense Mutation | CCT,GCT | P,A 101 | XP_005263696.1 | |
XM_011510965.1 | 712 | Missense Mutation | CCT,GCT | P,A 101 | XP_011509267.1 | |
XM_017003806.1 | 712 | Missense Mutation | CCT,GCT | P,A 101 | XP_016859295.1 |