Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCATGGGTTGGAGGGCCGGCGTCC[A/G]CATAAAATCCAGCTTCACATCCAAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614797 | ||||||||||||||||||||
Literature Links: |
PELI1 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 |
PELI1 - pellino E3 ubiquitin protein ligase 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020651.3 | 2183 | Missense Mutation | GCG,GTG | A,V 355 | NP_065702.2 | |
XM_005264437.3 | 2183 | Missense Mutation | GCG,GTG | A,V 257 | XP_005264494.1 | |
XM_011532994.2 | 2183 | Missense Mutation | GCG,GTG | A,V 355 | XP_011531296.1 | |
XM_011532996.2 | 2183 | Missense Mutation | GCG,GTG | A,V 257 | XP_011531298.1 | |
XM_011532997.2 | 2183 | Missense Mutation | GCG,GTG | A,V 176 | XP_011531299.1 | |
XM_017004520.1 | 2183 | Missense Mutation | GCG,GTG | A,V 355 | XP_016860009.1 | |
XM_017004521.1 | 2183 | Missense Mutation | GCG,GTG | A,V 289 | XP_016860010.1 |