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F5
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
79 submissions
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Phenotype: |
MIM: 612309
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Literature Links: |
F5 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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| F5 - coagulation factor V | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_000130.4 | 1746 | Missense Mutation | CAA,CGA | Q,R 534 | NP_000121.2 | |
| XM_017000660.1 | 1746 | Missense Mutation | CAA,CGA | Q,R 397 | XP_016856149.1 | |
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Set Membership: |
HapMap
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Panther Classification:
Gene Ontology Categories:
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