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AGGCAGTGAACAATAGCTATTGCCA[C/G]TTTGGAGCAATTTCCTTATGTGAAG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 308385 MIM: 430000 | |||||||||||||||||||||||
Literature Links: |
IL3RA PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
|
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 |
IL3RA - interleukin 3 receptor subunit alpha | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267713.1 | 594 | Intron | NP_001254642.1 | |||
NM_002183.3 | 594 | Missense Mutation | CAC,CAG | H,Q 69 | NP_002174.1 | |
XM_005274431.4 | 594 | Missense Mutation | CAC,CAG | H,Q 69 | XP_005274488.1 | |
XM_005274432.1 | 594 | Missense Mutation | CAC,CAG | H,Q 69 | XP_005274489.1 | |
XM_017029491.1 | 594 | Missense Mutation | CAC,CAG | H,Q 69 | XP_016884980.1 |