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GCTGCTGGGCCTCCTCCTGCAAGCC[C/T]GCACGCTCCTGCTGTAGCATAAGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605678 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MLXIPL 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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MLXIPL - MLX interacting protein like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032951.2 | 2172 | Silent Mutation | GCA,GCG | A,A 708 | NP_116569.1 | |
NM_032952.2 | 2172 | Silent Mutation | GCA,GCG | A,A 689 | NP_116570.1 | |
NM_032953.2 | 2172 | Silent Mutation | GCA,GCG | A,A 706 | NP_116571.1 | |
NM_032954.2 | 2172 | Silent Mutation | GCA,GCG | A,A 687 | NP_116572.1 | |
XM_011516277.1 | 2172 | Silent Mutation | GCA,GCG | A,A 773 | XP_011514579.1 | |
XM_011516278.1 | 2172 | Silent Mutation | GCA,GCG | A,A 772 | XP_011514580.1 | |
XM_011516279.1 | 2172 | Silent Mutation | GCA,GCG | A,A 755 | XP_011514581.1 | |
XM_011516281.2 | 2172 | Silent Mutation | GCA,GCG | A,A 432 | XP_011514583.1 | |
XM_017012263.1 | 2172 | Silent Mutation | GCA,GCG | A,A 405 | XP_016867752.1 |