Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATATAGGATAGGGCACTACAGATTC[C/T]GGTACAGTGACACCCTGGAGCTGGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 147045 | ||||||||||||||||||||
Literature Links: |
FCAR 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 |
FCAR - Fc fragment of IgA, receptor for | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002000.2 | 489 | Missense Mutation | CGG,TGG | R,W 110 | NP_001991.1 | |
NM_133269.2 | 489 | Missense Mutation | CGG,TGG | R,W 110 | NP_579803.1 | |
NM_133271.2 | 489 | Missense Mutation | CGG,TGG | R,W 110 | NP_579805.1 | |
NM_133272.2 | 489 | Missense Mutation | CGG,TGG | R,W 98 | NP_579806.1 | |
NM_133273.2 | 489 | Missense Mutation | CGG,TGG | R,W 98 | NP_579807.1 | |
NM_133274.2 | 489 | Missense Mutation | CGG,TGG | R,W 98 | NP_579808.1 | |
NM_133277.2 | 489 | Intron | NP_579811.1 | |||
NM_133278.2 | 489 | Missense Mutation | CGG,TGG | R,W 98 | NP_579812.1 | |
NM_133279.2 | 489 | Missense Mutation | CGG,TGG | R,W 110 | NP_579813.1 |