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CCACGAAGCCCAGGATGCTGATCAG[A/G]GCGTCCTTGAAGATGGTGAGGGGGC
Species: |
Human | |||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 608331 | |||||||||||||||||||||||||||||||||||
Literature Links: |
SLC36A2 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 | |||
AMR
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EUR - Not Available |
SLC36A2 - solute carrier family 36 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181776.2 | 1373 | Silent Mutation | GCC,GCT | A,A 445 | NP_861441.2 | |
XM_005268377.3 | 1373 | Intron | XP_005268434.1 | |||
XM_006714756.3 | 1373 | Silent Mutation | GCC,GCT | A,A 412 | XP_006714819.1 | |
XM_017009083.1 | 1373 | Intron | XP_016864572.1 | |||
XM_017009084.1 | 1373 | Silent Mutation | GCC,GCT | A,A 247 | XP_016864573.1 |