Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCTCTCTGATCTACTACAATCACAG[T/C]CATGATGGTCTGAATCACCAAGGCA
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 |
---|---|---|
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 |
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 | 1430 | Missense Mutation | ACT,GCT | T,A 422 | NP_079519.1 | |
XM_005246874.3 | 1430 | Missense Mutation | ACT,GCT | T,A 418 | XP_005246931.1 | |
XM_011511931.2 | 1430 | Missense Mutation | ACT,GCT | T,A 434 | XP_011510233.1 | |
XM_011511932.1 | 1430 | Missense Mutation | ACT,GCT | T,A 422 | XP_011510234.1 | |
XM_011511933.1 | 1430 | Missense Mutation | ACT,GCT | T,A 422 | XP_011510235.1 | |
XM_017005030.1 | 1430 | Missense Mutation | ACT,GCT | T,A 502 | XP_016860519.1 | |
XM_017005031.1 | 1430 | Missense Mutation | ACT,GCT | T,A 495 | XP_016860520.1 | |
XM_017005032.1 | 1430 | Missense Mutation | ACT,GCT | T,A 490 | XP_016860521.1 | |
XM_017005033.1 | 1430 | Missense Mutation | ACT,GCT | T,A 490 | XP_016860522.1 | |
XM_017005034.1 | 1430 | Missense Mutation | ACT,GCT | T,A 490 | XP_016860523.1 |