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- SNP ID:
- rs17795657
- Gene
-
LGALS13 - Gene Name
- Set Membership:
- > HapMap
- Chromosome Location:
- Chr.19: 39607050 - 39607050 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
GAAACATTAGAAATAAAGTCGGGTA[C/T]TGTCTCAAATAGGCACAAAACGTCA
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608717
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Literature Links: |
LGALS13 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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| LGALS13 - galectin 13 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_013268.2 | Intron | NP_037400.1 | ||||
| XM_011526874.2 | Intron | XP_011525176.1 | ||||
| XM_017026715.1 | Intron | XP_016882204.1 | ||||
Back To TopMore Information
Set Membership: |
HapMap
|
Panther Classification:
Gene Ontology Categories:
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