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- SNP ID:
- rs74683588
- Gene
-
MR1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.1: 181061693 - 181061693 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
AGTCTGTTTGCATGATGCCTTGTAC[A/G]TAGTAGCAACTCAGTAAATACTTTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 submissions
|
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Phenotype: |
MIM: 600764
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Literature Links: |
MR1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| MR1 - major histocompatibility complex, class I-related | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001194999.1 | 7574 | UTR 3 | NP_001181928.1 | |||
| NM_001195000.1 | 7574 | UTR 3 | NP_001181929.1 | |||
| NM_001195035.1 | 7574 | UTR 3 | NP_001181964.1 | |||
| NM_001310213.1 | 7574 | UTR 3 | NP_001297142.1 | |||
| NM_001531.2 | 7574 | UTR 3 | NP_001522.1 | |||
| XM_006711286.3 | 7574 | UTR 3 | XP_006711349.1 | |||
| XM_011509463.2 | 7574 | UTR 3 | XP_011507765.1 | |||
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