Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACTCCTGTGGTGCAGGCCATCTCCC[A/G]GATAGAGTGCATGGCCAGTTGGGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611367 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNPEP 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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DNPEP - aspartyl aminopeptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319116.1 | 1395 | Missense Mutation | CGG,TGG | R,W 461 | NP_001306045.1 | |
NM_001319117.1 | 1395 | Missense Mutation | CGG,TGG | R,W 425 | NP_001306046.1 | |
NM_001319118.1 | 1395 | Missense Mutation | CGG,TGG | R,W 439 | NP_001306047.1 | |
NM_001319119.1 | 1395 | Missense Mutation | CGG,TGG | R,W 439 | NP_001306048.1 | |
NM_001319120.1 | 1395 | Missense Mutation | CGG,TGG | R,W 417 | NP_001306049.1 | |
NM_001319121.1 | 1395 | Missense Mutation | CGG,TGG | R,W 400 | NP_001306050.1 | |
NM_001319122.1 | 1395 | Missense Mutation | CGG,TGG | R,W 400 | NP_001306051.1 | |
NM_012100.3 | 1395 | Missense Mutation | CGG,TGG | R,W 453 | NP_036232.2 |