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TTGGGGTTCAAATTCCAGTCTTTGA[C/T]TTACTGGTTGGGCAGGACACTTAGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610387 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SLC25A37 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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SLC25A37 - solute carrier family 25 member 37 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317812.1 | Intron | NP_001304741.1 | ||||
NM_001317813.1 | Intron | NP_001304742.1 | ||||
NM_001317814.1 | Intron | NP_001304743.1 | ||||
NM_016612.3 | Intron | NP_057696.2 | ||||
XM_006716352.3 | Intron | XP_006716415.1 | ||||
XM_011544550.2 | Intron | XP_011542852.1 | ||||
XM_011544553.2 | Intron | XP_011542855.1 | ||||
XM_011544554.2 | Intron | XP_011542856.1 | ||||
XM_017013532.1 | Intron | XP_016869021.1 |