SLC1A1
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 133550
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Literature Links: |
SLC1A1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap |
|---|---|---|
| Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
| EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
| SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
| AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
| EUR - Not Available | ||
| AMR - Not Available |
| SLC1A1 - solute carrier family 1 member 1 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_004170.5 | 1391 | Missense Mutation | TAT,TCT | Y,S 373 | NP_004161.4 | |
| XM_011518007.1 | 1391 | Missense Mutation | TAT,TCT | Y,S 396 | XP_011516309.1 | |
| XM_011518008.2 | 1391 | Missense Mutation | TAT,TCT | Y,S 376 | XP_011516310.1 | |
| XM_011518009.2 | 1391 | Missense Mutation | TAT,TCT | Y,S 353 | XP_011516311.1 | |
| XM_011518010.1 | 1391 | Missense Mutation | TAT,TCT | Y,S 326 | XP_011516312.1 | |
| XM_017015042.1 | 1391 | Missense Mutation | TAT,TCT | Y,S 360 | XP_016870531.1 | |
| XM_017015043.1 | 1391 | Missense Mutation | TAT,TCT | Y,S 337 | XP_016870532.1 | |
| SPATA6L - spermatogenesis associated 6 like | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001039395.3 | 1391 | Intron | NP_001034484.3 | |||
| XM_006716795.2 | 1391 | Intron | XP_006716858.1 | |||
| XM_006716798.3 | 1391 | Intron | XP_006716861.1 | |||
| XM_006716799.3 | 1391 | Intron | XP_006716862.1 | |||
| XM_006716800.2 | 1391 | Intron | XP_006716863.1 | |||
| XM_006716801.2 | 1391 | Intron | XP_006716864.1 | |||
| XM_011517952.1 | 1391 | Intron | XP_011516254.1 | |||
| XM_011517954.1 | 1391 | Intron | XP_011516256.1 | |||
| XM_011517956.1 | 1391 | Intron | XP_011516258.1 | |||
| XM_011517957.1 | 1391 | Intron | XP_011516259.1 | |||
| XM_011517958.1 | 1391 | Intron | XP_011516260.1 | |||
| XM_017014881.1 | 1391 | Intron | XP_016870370.1 | |||
| XM_017014882.1 | 1391 | Intron | XP_016870371.1 | |||
| XM_017014883.1 | 1391 | Intron | XP_016870372.1 | |||
| XM_017014884.1 | 1391 | Intron | XP_016870373.1 | |||
| XM_017014885.1 | 1391 | Intron | XP_016870374.1 | |||
| XM_017014886.1 | 1391 | Intron | XP_016870375.1 | |||
| XM_017014887.1 | 1391 | Intron | XP_016870376.1 | |||
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