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ATTCCTTCCCAATCACATCCCTGCA[C/G]GTCAGGTGGTAATTGTTGAGCCAGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602443 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
XPNPEP1 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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XPNPEP1 - X-prolyl aminopeptidase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001167604.1 | 1869 | Silent Mutation | ACC,ACG | T,T 610 | NP_001161076.1 | |
NM_001324128.1 | 1869 | Silent Mutation | ACC,ACG | T,T 520 | NP_001311057.1 | |
NM_001324131.1 | 1869 | Silent Mutation | ACC,ACG | T,T 503 | NP_001311060.1 | |
NM_001324132.1 | 1869 | Silent Mutation | ACC,ACG | T,T 591 | NP_001311061.1 | |
NM_001324133.1 | 1869 | Missense Mutation | CTG,GTG | L,V 654 | NP_001311062.1 | |
NM_001324134.1 | 1869 | Silent Mutation | ACC,ACG | T,T 460 | NP_001311063.1 | |
NM_001324135.1 | 1869 | Silent Mutation | ACC,ACG | T,T 617 | NP_001311064.1 | |
NM_001324136.1 | 1869 | Silent Mutation | ACC,ACG | T,T 629 | NP_001311065.1 | |
NM_020383.3 | 1869 | Silent Mutation | ACC,ACG | T,T 634 | NP_065116.3 | |
XM_011540134.1 | 1869 | Silent Mutation | ACC,ACG | T,T 576 | XP_011538436.1 | |
XM_017016613.1 | 1869 | Silent Mutation | ACC,ACG | T,T 586 | XP_016872102.1 | |
XM_017016614.1 | 1869 | Silent Mutation | ACC,ACG | T,T 520 | XP_016872103.1 | |
XM_017016615.1 | 1869 | Silent Mutation | ACC,ACG | T,T 520 | XP_016872104.1 |