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- SNP ID:
- rs17004659
- Gene
-
TSPEARTSPEAR-AS1TSPEAR-AS2 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.21: 44517319 - 44517319 on Build GRCh38
- Polymorphism:
- A/G, Transition substitution
- Context Sequence [VIC/FAM]:
TGCCAGTGCACCCCCCAGGAACACC[A/G]CCTAGTCCAGGGCTCCCACAGGTCT
Genomic Map
Back To TopAssay Details
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612920
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Literature Links: |
TSPEAR PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | ||||||
|---|---|---|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | ||||||
EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
|
| TSPEAR - thrombospondin type laminin G domain and EAR repeats | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001272037.1 | Intron | NP_001258966.1 | ||||
| NM_144991.2 | Intron | NP_659428.2 | ||||
| TSPEAR-AS1 - TSPEAR antisense RNA 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
| TSPEAR-AS2 - TSPEAR antisense RNA 2 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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