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CCCTCTCCAGCCCGGGGACTCAGCC[A/G]TTCATTCCTCCAGGATCCCTGGGTA
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606371 MIM: 600447 MIM: 604643 MIM: 605053 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
ATF7 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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ATF7 - activating transcription factor 7 | ||||||
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There are no transcripts associated with this gene. |
LOC100652999 - uncharacterized LOC100652999 | ||||||
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There are no transcripts associated with this gene. |
MAP3K12 - mitogen-activated protein kinase kinase kinase 12 | ||||||
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There are no transcripts associated with this gene. |
NPFF - neuropeptide FF-amide peptide precursor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320296.1 | 656 | Missense Mutation | CGG,TGG | R,W 91 | NP_001307225.1 | |
NM_003717.3 | 656 | Missense Mutation | CGG,TGG | R,W 88 | NP_003708.1 |
TARBP2 - TARBP2, RISC loading complex RNA binding subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_004178.4 | 656 | Intron | NP_004169.3 | |||
NM_134323.1 | 656 | Intron | NP_599150.1 | |||
NM_134324.2 | 656 | Intron | NP_599151.2 | |||
XM_005269114.1 | 656 | Intron | XP_005269171.1 | |||
XM_005269115.2 | 656 | Intron | XP_005269172.1 | |||
XM_005269117.1 | 656 | Intron | XP_005269174.1 | |||
XM_005269120.4 | 656 | Intron | XP_005269177.1 | |||
XM_005269122.3 | 656 | Intron | XP_005269179.1 | |||
XM_006719581.1 | 656 | Intron | XP_006719644.1 | |||
XM_011538712.2 | 656 | Intron | XP_011537014.1 | |||
XM_017019910.1 | 656 | Intron | XP_016875399.1 | |||
XM_017019911.1 | 656 | Intron | XP_016875400.1 |