Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGAGGAAAGTCTCTTCAGAGGAGC[A/G]TCCATGGGTGCTGTTCCCCTTGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 173391 | ||||||||||||||||||||
Literature Links: |
PLAUR 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 |
PLAUR - plasminogen activator, urokinase receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001005376.2 | 727 | Missense Mutation | CGC,TGC | R,C 227 | NP_001005376.1 | |
NM_001005377.2 | 727 | Missense Mutation | CGC,TGC | R,C 182 | NP_001005377.1 | |
NM_001301037.1 | 727 | Intron | NP_001287966.1 | |||
NM_002659.3 | 727 | Missense Mutation | CGC,TGC | R,C 227 | NP_002650.1 | |
XM_005258990.4 | 727 | Missense Mutation | CGC,TGC | R,C 227 | XP_005259047.1 | |
XM_011527027.2 | 727 | Missense Mutation | CGC,TGC | R,C 179 | XP_011525329.1 | |
XM_011527028.2 | 727 | Silent Mutation | GAC,GAT | D,D 233 | XP_011525330.1 | |
XM_011527029.1 | 727 | Silent Mutation | GAC,GAT | D,D 233 | XP_011525331.1 | |
XM_011527030.2 | 727 | Intron | XP_011525332.1 | |||
XM_011527031.2 | 727 | Intron | XP_011525333.1 | |||
XM_017026872.1 | 727 | Missense Mutation | CGC,TGC | R,C 222 | XP_016882361.1 | |
XM_017026873.1 | 727 | Missense Mutation | CGC,TGC | R,C 103 | XP_016882362.1 |