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MYO15B
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MYO15B 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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| MYO15B - myosin XVB | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001309242.1 | 2397 | Silent Mutation | CGA,CGG | R,R 846 | NP_001296171.1 | |
| XM_017025120.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880609.1 | |
| XM_017025121.1 | 2397 | Silent Mutation | CGA,CGG | R,R 623 | XP_016880610.1 | |
| XM_017025122.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880611.1 | |
| XM_017025123.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880612.1 | |
| XM_017025124.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880613.1 | |
| XM_017025125.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880614.1 | |
| XM_017025126.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880615.1 | |
| XM_017025127.1 | 2397 | Silent Mutation | CGA,CGG | R,R 399 | XP_016880616.1 | |
| XM_017025128.1 | 2397 | Silent Mutation | CGA,CGG | R,R 390 | XP_016880617.1 | |
| XM_017025129.1 | 2397 | Silent Mutation | CGA,CGG | R,R 107 | XP_016880618.1 | |
| XM_017025130.1 | 2397 | Silent Mutation | CGA,CGG | R,R 99 | XP_016880619.1 | |
| XM_017025131.1 | 2397 | Silent Mutation | CGA,CGG | R,R 64 | XP_016880620.1 | |
| XM_017025132.1 | 2397 | UTR 5 | XP_016880621.1 | |||
| XM_017025133.1 | 2397 | UTR 5 | XP_016880622.1 | |||
| XM_017025134.1 | 2397 | UTR 5 | XP_016880623.1 | |||
| XM_017025135.1 | 2397 | Intron | XP_016880624.1 | |||
| XM_017025136.1 | 2397 | Intron | XP_016880625.1 | |||
| XM_017025137.1 | 2397 | Intron | XP_016880626.1 | |||
| XM_017025138.1 | 2397 | Intron | XP_016880627.1 | |||
| XM_017025139.1 | 2397 | Intron | XP_016880628.1 | |||
| XM_017025140.1 | 2397 | Intron | XP_016880629.1 | |||
| XM_017025141.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880630.1 | |
| XM_017025142.1 | 2397 | Silent Mutation | CGA,CGG | R,R 628 | XP_016880631.1 | |
| XM_017025143.1 | 2397 | Intron | XP_016880632.1 | |||
| XM_017025144.1 | 2397 | UTR 5 | XP_016880633.1 | |||
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