Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCCTGGCGGCCCTGTTTCTGCAATT[C/T]CTTCCCAATCACATCCCTGCAGGTC
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 |
---|---|---|
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 |
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 | 1891 | Missense Mutation | AAA,GAA | K,E 618 | NP_001161076.1 | |
NM_001324128.1 | 1891 | Missense Mutation | AAA,GAA | K,E 528 | NP_001311057.1 | |
NM_001324131.1 | 1891 | Missense Mutation | AAA,GAA | K,E 511 | NP_001311060.1 | |
NM_001324132.1 | 1891 | Missense Mutation | AAA,GAA | K,E 599 | NP_001311061.1 | |
NM_001324133.1 | 1891 | Missense Mutation | GAA,GGA | E,G 661 | NP_001311062.1 | |
NM_001324134.1 | 1891 | Missense Mutation | AAA,GAA | K,E 468 | NP_001311063.1 | |
NM_001324135.1 | 1891 | Missense Mutation | AAA,GAA | K,E 625 | NP_001311064.1 | |
NM_001324136.1 | 1891 | Missense Mutation | AAA,GAA | K,E 637 | NP_001311065.1 | |
NM_020383.3 | 1891 | Missense Mutation | AAA,GAA | K,E 642 | NP_065116.3 | |
XM_011540134.1 | 1891 | Missense Mutation | AAA,GAA | K,E 584 | XP_011538436.1 | |
XM_017016613.1 | 1891 | Missense Mutation | AAA,GAA | K,E 594 | XP_016872102.1 | |
XM_017016614.1 | 1891 | Missense Mutation | AAA,GAA | K,E 528 | XP_016872103.1 | |
XM_017016615.1 | 1891 | Missense Mutation | AAA,GAA | K,E 528 | XP_016872104.1 |