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ATATGTGAGCCTGTCTCCTTAGCAC[A/G]AGAGAGAATATTTCCCTCACTATTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
SLC37A3 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 |
SLC37A3 - solute carrier family 37 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287498.1 | 1950 | Silent Mutation | CTC,CTT | L,L 467 | NP_001274427.1 | |
NM_032295.3 | 1950 | Missense Mutation | CGT,TGT | R,C 383 | NP_115671.1 | |
NM_207113.2 | 1950 | Silent Mutation | CTC,CTT | L,L 483 | NP_996996.1 | |
XM_011516626.2 | 1950 | Missense Mutation | CGT,TGT | R,C 433 | XP_011514928.1 | |
XM_011516627.2 | 1950 | Missense Mutation | CGT,TGT | R,C 417 | XP_011514929.1 | |
XM_017012712.1 | 1950 | Silent Mutation | CTC,CTT | L,L 483 | XP_016868201.1 | |
XM_017012713.1 | 1950 | Missense Mutation | CGT,TGT | R,C 383 | XP_016868202.1 | |
XM_017012714.1 | 1950 | Silent Mutation | CTC,CTT | L,L 402 | XP_016868203.1 | |
XM_017012715.1 | 1950 | Silent Mutation | CTC,CTT | L,L 395 | XP_016868204.1 | |
XM_017012716.1 | 1950 | Missense Mutation | CGT,TGT | R,C 295 | XP_016868205.1 | |
XM_017012717.1 | 1950 | Silent Mutation | CTC,CTT | L,L 335 | XP_016868206.1 | |
XM_017012718.1 | 1950 | Intron | XP_016868207.1 |