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TTACGTCACTTTCTTCCTTTTTGTG[C/T]GTTTTGTGCAGCCCCTGCCAAACCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602020 MIM: 607996 MIM: 602679 MIM: 606212 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MAFG 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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MAFG - MAF bZIP transcription factor G | ||||||
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There are no transcripts associated with this gene. |
NPB - neuropeptide B | ||||||
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There are no transcripts associated with this gene. |
PCYT2 - phosphate cytidylyltransferase 2, ethanolamine | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184917.2 | 2832 | Intron | NP_001171846.1 | |||
NM_001256433.2 | 2832 | Intron | NP_001243362.1 | |||
NM_001256434.2 | 2832 | Intron | NP_001243363.1 | |||
NM_001256435.2 | 2832 | Intron | NP_001243364.1 | |||
NM_001282203.1 | 2832 | Intron | NP_001269132.1 | |||
NM_001282204.1 | 2832 | Intron | NP_001269133.1 | |||
NM_002861.4 | 2832 | Intron | NP_002852.1 | |||
XM_005256386.3 | 2832 | Intron | XP_005256443.1 | |||
XM_005256387.3 | 2832 | Intron | XP_005256444.1 | |||
XM_006722287.3 | 2832 | Intron | XP_006722350.1 | |||
XM_017024910.1 | 2832 | Intron | XP_016880399.1 | |||
XM_017024911.1 | 2832 | Intron | XP_016880400.1 | |||
XM_017024912.1 | 2832 | Intron | XP_016880401.1 |
SIRT7 - sirtuin 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016538.2 | 2832 | Missense Mutation | NP_057622.1 | |||
XM_006722284.2 | 2832 | Missense Mutation | XP_006722347.1 | |||
XM_011523580.1 | 2832 | Missense Mutation | XP_011521882.1 | |||
XM_011523581.2 | 2832 | Missense Mutation | XP_011521883.1 |