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AGAATGTGCACTGAGGGAGCGTTTC[C/T]GCACAGATCTGCGTGTTCCTTACCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 605687 | ||||||||||||||||||||
Literature Links: |
IL19 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
IL19 - interleukin 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_013371.3 | 48 | Intron | NP_037503.2 | |||
NM_153758.2 | 48 | Missense Mutation | CCG,CTG | P,L 8 | NP_715639.1 | |
XM_011509450.2 | 48 | Intron | XP_011507752.1 |