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GCCAGGGGGCTCGCAGCCCTGAGAG[C/T]GACTCCATTCAGTGGTTCCACAATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
14 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 | |||
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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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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 | 248 | Silent Mutation | AGC,AGT | S,S 70 | NP_001129691.1 | |
NM_021642.3 | 248 | Silent Mutation | AGC,AGT | S,S 69 | NP_067674.2 | |
XM_011509287.2 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_011507589.1 | |
XM_011509290.2 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_011507592.1 | |
XM_011509291.1 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_011507593.1 | |
XM_017000663.1 | 248 | Silent Mutation | AGC,AGT | S,S 69 | XP_016856152.1 | |
XM_017000664.1 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_016856153.1 | |
XM_017000665.1 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_016856154.1 | |
XM_017000666.1 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_016856155.1 | |
XM_017000667.1 | 248 | Silent Mutation | AGC,AGT | S,S 70 | XP_016856156.1 | |
XM_017000668.1 | 248 | Silent Mutation | AGC,AGT | S,S 69 | XP_016856157.1 |