Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTGAGAGAGACTAATAGATTTTGCT[C/G]TAAGGTATAAAATCCATTATCTGAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608490 | ||||||||||||||||||||
Literature Links: |
SLC38A1 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 |
SLC38A1 - solute carrier family 38 member 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077484.1 | 6699 | UTR 3 | NP_001070952.1 | |||
NM_001278387.1 | 6699 | UTR 3 | NP_001265316.1 | |||
NM_001278388.1 | 6699 | UTR 3 | NP_001265317.1 | |||
NM_001278389.1 | 6699 | UTR 3 | NP_001265318.1 | |||
NM_001278390.1 | 6699 | Intron | NP_001265319.1 | |||
NM_030674.3 | 6699 | UTR 3 | NP_109599.3 | |||
XM_011538784.2 | 6699 | Intron | XP_011537086.1 | |||
XM_011538786.2 | 6699 | Intron | XP_011537088.1 | |||
XM_011538787.2 | 6699 | Intron | XP_011537089.1 | |||
XM_017019990.1 | 6699 | Intron | XP_016875479.1 |