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- SNP ID:
- rs10987248
- Gene
-
MVB12B - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.9: 126332084 - 126332084 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TGTTTCAGAGCCCATCTGCTCCTTG[C/T]AGTTCCCCGAGCAGTCCCTGTGTGT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MVB12B 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
|
| MVB12B - multivesicular body subunit 12B | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001011703.2 | Intron | NP_001011703.1 | ||||
| NM_033446.2 | Intron | NP_258257.1 | ||||
| XM_005252297.1 | Intron | XP_005252354.1 | ||||
| XM_017015275.1 | Intron | XP_016870764.1 | ||||
| XM_017015276.1 | Intron | XP_016870765.1 | ||||
| XM_017015277.1 | Intron | XP_016870766.1 | ||||
| XM_017015278.1 | Intron | XP_016870767.1 | ||||
| XM_017015279.1 | Intron | XP_016870768.1 | ||||
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HapMap