Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGGTTCGGGCCACATCACTGTGGC[C/T]CACCAGCAGGTAGTTGGGAGTCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
13 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 | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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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 | 1399 | Missense Mutation | AGC,GGC | S,G 347 | NP_065126.2 | |
XM_011509789.2 | 1399 | Missense Mutation | AGC,GGC | S,G 347 | XP_011508091.1 | |
XM_011509790.1 | 1399 | Missense Mutation | AGC,GGC | S,G 347 | XP_011508092.1 | |
XM_011509791.2 | 1399 | Missense Mutation | AGC,GGC | S,G 343 | XP_011508093.1 | |
XM_011509792.1 | 1399 | Intron | XP_011508094.1 | |||
XM_011509793.2 | 1399 | Missense Mutation | AGC,GGC | S,G 179 | XP_011508095.1 |