Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CCGAGAAGCCAAGATAGGTCCAATG[A/G]TGGTTCCACAGGGGGTGTCATTCCG
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 |
---|---|---|
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 |
DNPEP - aspartyl aminopeptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319116.1 | 1315 | Missense Mutation | ACC,ATC | T,I 434 | NP_001306045.1 | |
NM_001319117.1 | 1315 | Missense Mutation | ACC,ATC | T,I 398 | NP_001306046.1 | |
NM_001319118.1 | 1315 | Missense Mutation | ACC,ATC | T,I 412 | NP_001306047.1 | |
NM_001319119.1 | 1315 | Missense Mutation | ACC,ATC | T,I 412 | NP_001306048.1 | |
NM_001319120.1 | 1315 | Missense Mutation | ACC,ATC | T,I 390 | NP_001306049.1 | |
NM_001319121.1 | 1315 | Missense Mutation | ACC,ATC | T,I 373 | NP_001306050.1 | |
NM_001319122.1 | 1315 | Missense Mutation | ACC,ATC | T,I 373 | NP_001306051.1 | |
NM_012100.3 | 1315 | Missense Mutation | ACC,ATC | T,I 426 | NP_036232.2 |