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CGTGAGCTCCCGGAGTCATGTGACC[A/G]CCGTCTTGACAGTGTTCCACGGGCG
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MFSD1 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 - 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 |
MFSD1 - major facilitator superfamily domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167903.1 | 141 | Missense Mutation | ACC,GCC | T,A 21 | NP_001161375.1 | |
NM_001289406.1 | 141 | UTR 5 | NP_001276335.1 | |||
NM_001289407.1 | 141 | UTR 5 | NP_001276336.1 | |||
NM_022736.2 | 141 | Missense Mutation | ACC,GCC | T,A 21 | NP_073573.2 | |
XM_006713730.2 | 141 | Missense Mutation | ACC,GCC | T,A 21 | XP_006713793.1 |