Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCAAAAGTTTCTCAGTGCTGCTTTC[C/T]CGCACTGTCATAGAAATCTCTGATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 176785 | ||||||||||||||||||||
Literature Links: |
PRCP 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 |
PRCP - prolylcarboxypeptidase | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001319214.1 | 1741 | Missense Mutation | AGA,GGA | R,G 388 | NP_001306143.1 | |
NM_005040.3 | 1741 | Missense Mutation | AGA,GGA | R,G 493 | NP_005031.1 | |
NM_199418.3 | 1741 | Missense Mutation | AGA,GGA | R,G 514 | NP_955450.2 | |
XM_005274093.1 | 1741 | Missense Mutation | AGA,GGA | R,G 388 | XP_005274150.1 |