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CCCACTAATCCTGATGAGGCTGACA[A/G]AGTTGGGGTGAGTGATCCCAGCCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
20 submissions
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Phenotype: |
MIM: 604590 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FCGR2B 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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FCGR2B - Fc fragment of IgG receptor IIb | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002273.2 | 975 | Missense Mutation | AAA,AGA | K,R 263 | NP_001002273.1 | |
NM_001002274.2 | 975 | Missense Mutation | AAA,AGA | K,R 264 | NP_001002274.1 | |
NM_001002275.2 | 975 | Missense Mutation | AAA,AGA | K,R 282 | NP_001002275.1 | |
NM_001190828.1 | 975 | Missense Mutation | AAA,AGA | K,R 276 | NP_001177757.1 | |
NM_004001.4 | 975 | Missense Mutation | AAA,AGA | K,R 283 | NP_003992.3 | |
XM_011509292.2 | 975 | Intron | XP_011507594.1 | |||
XM_017000669.1 | 975 | Intron | XP_016856158.1 | |||
XM_017000670.1 | 975 | Intron | XP_016856159.1 | |||
XM_017000671.1 | 975 | Missense Mutation | AAA,AGA | K,R 283 | XP_016856160.1 | |
XM_017000672.1 | 975 | Missense Mutation | AAA,AGA | K,R 264 | XP_016856161.1 |
RPL31P11 - ribosomal protein L31 pseudogene 11 | ||||||
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There are no transcripts associated with this gene. |