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ACAGCAGAGGTAACATTTTAAAGGC[C/T]CAGCTAAGGAGCAAGCATGACTTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 600764 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MR1 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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MR1 - major histocompatibility complex, class I-related | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001194999.1 | Intron | NP_001181928.1 | ||||
NM_001195000.1 | Intron | NP_001181929.1 | ||||
NM_001195035.1 | Intron | NP_001181964.1 | ||||
NM_001310213.1 | Intron | NP_001297142.1 | ||||
NM_001531.2 | Intron | NP_001522.1 | ||||
XM_006711286.3 | Intron | XP_006711349.1 | ||||
XM_011509463.2 | Intron | XP_011507765.1 |