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TCTGACATGCCAGGGGGCTCGCAGC[A/C]CTGAGAGCGACTCCATTCAGTGGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
2 submissions
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Phenotype: |
MIM: 146790 | ||||||||||||||||||||
Literature Links: |
FCGR2A 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 |
FCGR2A - Fc fragment of IgG receptor IIa | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001136219.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | NP_001129691.1 | |
NM_021642.3 | 240 | Missense Mutation | ACT,CCT | T,P 67 | NP_067674.2 | |
XM_011509287.2 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_011507589.1 | |
XM_011509290.2 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_011507592.1 | |
XM_011509291.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_011507593.1 | |
XM_017000663.1 | 240 | Missense Mutation | ACT,CCT | T,P 67 | XP_016856152.1 | |
XM_017000664.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_016856153.1 | |
XM_017000665.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_016856154.1 | |
XM_017000666.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_016856155.1 | |
XM_017000667.1 | 240 | Missense Mutation | ACT,CCT | T,P 68 | XP_016856156.1 | |
XM_017000668.1 | 240 | Missense Mutation | ACT,CCT | T,P 67 | XP_016856157.1 |