Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGTCACAAAAGTTCCGTGTGTCCA[C/T]GTGAAAGGACTGTATGTTTCGGACG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
12 submissions
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Phenotype: |
MIM: 608197 | ||||||||||||||||||||
Literature Links: |
PGLYRP3 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 |
PGLYRP3 - peptidoglycan recognition protein 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_052891.2 | 1176 | Missense Mutation | ATG,GTG | M,V 232 | NP_443123.1 | |
XM_011509118.1 | 1176 | Missense Mutation | ATG,GTG | M,V 268 | XP_011507420.1 | |
XM_011509119.1 | 1176 | Missense Mutation | ATG,GTG | M,V 232 | XP_011507421.1 | |
XM_011509120.2 | 1176 | Missense Mutation | ATG,GTG | M,V 230 | XP_011507422.1 |