Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109190 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC1A5 PubMed Links | |||||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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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 | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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SLC1A5 - solute carrier family 1 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145144.1 | 1208 | Missense Mutation | CTC,GTC | L,V 284 | NP_001138616.1 | |
NM_001145145.1 | 1208 | Missense Mutation | CTC,GTC | L,V 310 | NP_001138617.1 | |
NM_005628.2 | 1208 | Missense Mutation | CTC,GTC | L,V 512 | NP_005619.1 | |
XM_005259167.4 | 1208 | Intron | XP_005259224.1 |
Set Membership: |
HapMap |