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GCTGCGCGGCTACTACAATCAGAGC[A/G]AGGCCGGTGAGTGACCCCGGCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 143010 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HLA-E 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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HLA-E - major histocompatibility complex, class I, E | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005516.5 | 466 | Missense Mutation | AAG,GAG | K,E 110 | NP_005507.3 | |
XM_017010807.1 | 466 | Missense Mutation | AAG,GAG | K,E 151 | XP_016866296.1 | |
XM_017010808.1 | 466 | Missense Mutation | AAG,GAG | K,E 151 | XP_016866297.1 | |
XM_017010809.1 | 466 | Missense Mutation | AAG,GAG | K,E 110 | XP_016866298.1 |