Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTGCAGCGGCTCACTCACCTGCTA[C/T]AGGCGGGGATCTCCAAGCCCAGCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602020 MIM: 602679 MIM: 606212 | ||||||||||||||||||||
Literature Links: |
MAFG PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | 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 |
MAFG - MAF bZIP transcription factor G | ||||||
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There are no transcripts associated with this gene. |
PCYT2 - phosphate cytidylyltransferase 2, ethanolamine | ||||||
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There are no transcripts associated with this gene. |
SIRT7 - sirtuin 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016538.2 | 2652 | Missense Mutation | TAT,TGT | Y,C 333 | NP_057622.1 | |
XM_006722284.2 | 2652 | Missense Mutation | TAT,TGT | Y,C 251 | XP_006722347.1 | |
XM_011523580.1 | 2652 | Missense Mutation | TAT,TGT | Y,C 298 | XP_011521882.1 | |
XM_011523581.2 | 2652 | Missense Mutation | TAT,TGT | Y,C 262 | XP_011521883.1 |