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- SNP ID:
- rs9488343
- Gene
-
HS3ST5LOC101927768 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.6: 114226817 - 114226817 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
GTCTGATAAATACACCAATGATAAT[A/G]AACATGATTCACTTCAAGACACAAT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609407
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Literature Links: |
HS3ST5 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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| HS3ST5 - heparan sulfate-glucosamine 3-sulfotransferase 5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_153612.3 | Intron | NP_705840.2 | ||||
| XM_006715379.2 | Intron | XP_006715442.1 | ||||
| XM_011535588.2 | Intron | XP_011533890.1 | ||||
| XM_017010470.1 | Intron | XP_016865959.1 | ||||
| XM_017010471.1 | Intron | XP_016865960.1 | ||||
| XM_017010472.1 | Intron | XP_016865961.1 | ||||
| XM_017010473.1 | Intron | XP_016865962.1 | ||||
| XM_017010474.1 | Intron | XP_016865963.1 | ||||
| LOC101927768 - uncharacterized LOC101927768 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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