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CTCTGAAGCCAGCTACAAAAACTGC[A/G]GAACTGTCAGTTGTATCTACATCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 138440 MIM: 182465 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GART 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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GART - phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase | ||||||
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There are no transcripts associated with this gene. |
MIR6501 - microRNA 6501 | ||||||
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There are no transcripts associated with this gene. |
SON - SON DNA binding protein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291411.1 | 691 | Silent Mutation | GCA,GCG | A,A 212 | NP_001278340.1 | |
NM_001291412.1 | 691 | Intron | NP_001278341.1 | |||
NM_032195.2 | 691 | Silent Mutation | GCA,GCG | A,A 212 | NP_115571.2 | |
NM_138927.2 | 691 | Silent Mutation | GCA,GCG | A,A 212 | NP_620305.2 |