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GCAGGGTGAGCAGGAACCAGACCAG[C/T]GTCTGCAGCACTCGCCGCCGCCGCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614236 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC38A7 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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SLC38A7 - solute carrier family 38 member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001308384.1 | 1522 | Intron | NP_001295313.1 | |||
NM_018231.2 | 1522 | Silent Mutation | ACA,ACG | T,T 374 | NP_060701.1 | |
XM_017023393.1 | 1522 | Silent Mutation | ACA,ACG | T,T 374 | XP_016878882.1 | |
XM_017023394.1 | 1522 | Intron | XP_016878883.1 | |||
XM_017023395.1 | 1522 | Intron | XP_016878884.1 | |||
XM_017023396.1 | 1522 | Intron | XP_016878885.1 | |||
XM_017023397.1 | 1522 | Intron | XP_016878886.1 | |||
XM_017023398.1 | 1522 | Intron | XP_016878887.1 | |||
XM_017023399.1 | 1522 | Intron | XP_016878888.1 |