Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAAAGCCTGCCCAGGAGACAAGGTT[C/T]GGGCCACATCACTGTGGCCCACCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 608198 | ||||||||||||||||||||
Literature Links: |
PGLYRP4 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 |
PGLYRP4 - peptidoglycan recognition protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020393.3 | 1418 | Missense Mutation | CAA,CGA | Q,R 353 | NP_065126.2 | |
XM_011509789.2 | 1418 | Missense Mutation | CAA,CGA | Q,R 353 | XP_011508091.1 | |
XM_011509790.1 | 1418 | Missense Mutation | CAA,CGA | Q,R 353 | XP_011508092.1 | |
XM_011509791.2 | 1418 | Missense Mutation | CAA,CGA | Q,R 349 | XP_011508093.1 | |
XM_011509792.1 | 1418 | Intron | XP_011508094.1 | |||
XM_011509793.2 | 1418 | Missense Mutation | CAA,CGA | Q,R 185 | XP_011508095.1 |