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CGTGGCGGACAGCCGGCGGGCTTGG[C/G]GGGGGGCGGTGGGCGGCGATCCACC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611963 | ||||||||||||||||||||
Literature Links: |
LOC344967 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 |
LOC344967 - acyl-CoA thioesterase 7 pseudogene | ||||||
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There are no transcripts associated with this gene. |
N4BP2 - NEDD4 binding protein 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318359.1 | 485 | Intron | NP_001305288.1 | |||
NM_018177.5 | 485 | Intron | NP_060647.2 | |||
XM_006714023.3 | 485 | Intron | XP_006714086.1 | |||
XM_011513716.2 | 485 | Missense Mutation | GCG,GGG | A,G 101 | XP_011512018.1 | |
XM_011513717.2 | 485 | Missense Mutation | GCG,GGG | A,G 101 | XP_011512019.1 | |
XM_011513718.2 | 485 | Intron | XP_011512020.1 | |||
XM_011513719.2 | 485 | Intron | XP_011512021.1 | |||
XM_011513720.1 | 485 | Intron | XP_011512022.1 | |||
XM_011513721.1 | 485 | Intron | XP_011512023.1 | |||
XM_017008397.1 | 485 | Missense Mutation | GCG,GGG | A,G 101 | XP_016863886.1 | |
XM_017008398.1 | 485 | Intron | XP_016863887.1 | |||
XM_017008399.1 | 485 | Intron | XP_016863888.1 |