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- SNP ID:
- rs138758317
- Gene
-
SLC1A2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.11: 35252177 - 35252177 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
CTGTGCTTTCGTAGGGTTTCACCTG[C/T]AGATGCATTTGCAGTTAGTTAGTCA
Genomic Map
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Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 600300
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Literature Links: |
SLC1A2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
| SLC1A2 - solute carrier family 1 member 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001195728.2 | 11034 | UTR 3 | NP_001182657.1 | |||
| NM_001252652.1 | 11034 | UTR 3 | NP_001239581.1 | |||
| NM_004171.3 | 11034 | UTR 3 | NP_004162.2 | |||
| XM_005253067.1 | 11034 | UTR 3 | XP_005253124.1 | |||
| XM_011520285.2 | 11034 | UTR 3 | XP_011518587.1 | |||
| XM_017018136.1 | 11034 | UTR 3 | XP_016873625.1 | |||
| XM_017018137.1 | 11034 | UTR 3 | XP_016873626.1 | |||
| XM_017018138.1 | 11034 | UTR 3 | XP_016873627.1 | |||
| XM_017018139.1 | 11034 | UTR 3 | XP_016873628.1 | |||
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