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GCACGACTGGCACAGTGAGGGTCAC[C/T]GCGAGCAGCACGGCCAGGCGCACAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300649 | ||||||||||||||||||||
Literature Links: |
SLC38A5 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 |
SLC38A5 - solute carrier family 38 member 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033518.3 | 1213 | Silent Mutation | GCA,GCG | A,A 345 | NP_277053.2 | |
XM_005272694.3 | 1213 | Silent Mutation | GCA,GCG | A,A 392 | XP_005272751.2 | |
XM_005272695.4 | 1213 | Silent Mutation | GCA,GCG | A,A 392 | XP_005272752.3 | |
XM_005272697.2 | 1213 | Silent Mutation | GCA,GCG | A,A 351 | XP_005272754.2 | |
XM_005272698.4 | 1213 | Silent Mutation | GCA,GCG | A,A 345 | XP_005272755.2 | |
XM_006724569.3 | 1213 | Silent Mutation | GCA,GCG | A,A 345 | XP_006724632.1 | |
XM_017029960.1 | 1213 | Silent Mutation | GCA,GCG | A,A 351 | XP_016885449.1 | |
XM_017029961.1 | 1213 | Silent Mutation | GCA,GCG | A,A 345 | XP_016885450.1 |