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TCAGTTTTCCATCTGCACATATAAC[C/G]CCCATTCCTCCATGAATTGCATGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605620 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL20RA 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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IL20RA - interleukin 20 receptor subunit alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001278722.1 | 1910 | Missense Mutation | GCG,GGG | A,G 497 | NP_001265651.1 | |
NM_001278723.1 | 1910 | Missense Mutation | GCG,GGG | A,G 435 | NP_001265652.1 | |
NM_001278724.1 | 1910 | Missense Mutation | GCG,GGG | A,G 413 | NP_001265653.1 | |
NM_014432.3 | 1910 | Missense Mutation | GCG,GGG | A,G 546 | NP_055247.3 | |
XM_006715506.2 | 1910 | Missense Mutation | GCG,GGG | A,G 413 | XP_006715569.1 | |
XM_011535904.2 | 1910 | Missense Mutation | GCG,GGG | A,G 435 | XP_011534206.1 | |
XM_017010954.1 | 1910 | Missense Mutation | GCG,GGG | A,G 547 | XP_016866443.1 | |
XM_017010955.1 | 1910 | Missense Mutation | GCG,GGG | A,G 498 | XP_016866444.1 |
NHEG1 - neuroblastoma highly expressed 1 | ||||||
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There are no transcripts associated with this gene. |