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ACCACGGCATGTGTCTGTGAATGTC[C/T]GCAAAACATTGTGAGTATTGATTTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609510 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IL31RA 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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IL31RA - interleukin 31 receptor A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242636.1 | 245 | Intron | NP_001229565.1 | |||
NM_001242637.1 | 245 | Missense Mutation | CCG,CTG | P,L 18 | NP_001229566.1 | |
NM_001242638.1 | 245 | UTR 5 | NP_001229567.1 | |||
NM_001242639.1 | 245 | Intron | NP_001229568.1 | |||
NM_001297570.1 | 245 | Missense Mutation | CCG,CTG | P,L 18 | NP_001284499.1 | |
NM_001297572.1 | 245 | UTR 5 | NP_001284501.1 | |||
NM_139017.5 | 245 | Missense Mutation | CCG,CTG | P,L 18 | NP_620586.3 | |
XM_011543142.2 | 245 | Intron | XP_011541444.1 | |||
XM_011543143.2 | 245 | Intron | XP_011541445.1 | |||
XM_011543144.2 | 245 | Intron | XP_011541446.1 | |||
XM_011543145.2 | 245 | Intron | XP_011541447.1 |