Search Thermo Fisher Scientific
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CTACACGAAGGCCTCCTGGTTGGAC[C/G]AGCCGTTGATTTTGAGGAAGAGTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610791 | ||||||||||||||||||||
Literature Links: |
SLC43A2 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 |
SLC43A2 - solute carrier family 43 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284498.1 | 1824 | Missense Mutation | TCG,TGG | S,W 566 | NP_001271427.1 | |
NM_001284499.1 | 1824 | Missense Mutation | TCG,TGG | S,W 425 | NP_001271428.1 | |
NM_001321364.1 | 1824 | Missense Mutation | TCG,TGG | S,W 566 | NP_001308293.1 | |
NM_001321365.1 | 1824 | Missense Mutation | TCG,TGG | S,W 566 | NP_001308294.1 | |
NM_152346.2 | 1824 | Missense Mutation | TCG,TGG | S,W 562 | NP_689559.1 | |
XM_017024177.1 | 1824 | Missense Mutation | TCG,TGG | S,W 562 | XP_016879666.1 | |
XM_017024178.1 | 1824 | Missense Mutation | TCG,TGG | S,W 562 | XP_016879667.1 | |
XM_017024179.1 | 1824 | Missense Mutation | TCG,TGG | S,W 529 | XP_016879668.1 |