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AGAAGCATATAGCTGGACTTGAATA[C/T]CAAATAGCCAGCATAGCACGCCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606152 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC19A3 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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SLC19A3 - solute carrier family 19 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_025243.3 | 1298 | Missense Mutation | ATA,GTA | I,V 378 | NP_079519.1 | |
XM_005246874.3 | 1298 | Missense Mutation | ATA,GTA | I,V 374 | XP_005246931.1 | |
XM_011511931.2 | 1298 | Missense Mutation | ATA,GTA | I,V 390 | XP_011510233.1 | |
XM_011511932.1 | 1298 | Missense Mutation | ATA,GTA | I,V 378 | XP_011510234.1 | |
XM_011511933.1 | 1298 | Missense Mutation | ATA,GTA | I,V 378 | XP_011510235.1 | |
XM_017005030.1 | 1298 | Missense Mutation | ATA,GTA | I,V 458 | XP_016860519.1 | |
XM_017005031.1 | 1298 | Missense Mutation | ATA,GTA | I,V 451 | XP_016860520.1 | |
XM_017005032.1 | 1298 | Missense Mutation | ATA,GTA | I,V 446 | XP_016860521.1 | |
XM_017005033.1 | 1298 | Missense Mutation | ATA,GTA | I,V 446 | XP_016860522.1 | |
XM_017005034.1 | 1298 | Missense Mutation | ATA,GTA | I,V 446 | XP_016860523.1 |