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AAGCCCATGGGGAGCTCCAGACTGG[C/T]AGCCCTGCTCCTGCCTCTCCTCCTC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 614995 MIM: 616012 | |||||||||||||||||||||||
Literature Links: |
IL17RE 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 - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
IL17RE - interleukin 17 receptor E | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001193380.1 | 161 | Missense Mutation | GCA,GTA | A,V 7 | NP_001180309.1 | |
NM_153480.1 | 161 | Missense Mutation | GCA,GTA | A,V 7 | NP_705613.1 | |
NM_153481.1 | 161 | UTR 5 | NP_705614.1 | |||
NM_153483.2 | 161 | Missense Mutation | GCA,GTA | A,V 47 | NP_705616.2 | |
XM_006712975.1 | 161 | Missense Mutation | GCA,GTA | A,V 7 | XP_006713038.1 | |
XM_006712976.1 | 161 | UTR 5 | XP_006713039.1 | |||
XM_011533361.2 | 161 | Missense Mutation | GCA,GTA | A,V 53 | XP_011531663.1 | |
XM_011533362.2 | 161 | Missense Mutation | GCA,GTA | A,V 7 | XP_011531664.1 | |
XM_011533363.2 | 161 | Missense Mutation | GCA,GTA | A,V 7 | XP_011531665.1 | |
XM_011533364.2 | 161 | Missense Mutation | GCA,GTA | A,V 7 | XP_011531666.1 |
JAGN1 - jagunal homolog 1 | ||||||
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There are no transcripts associated with this gene. |