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CACATGGACGCAAACAAGGCAGGGC[A/G]CTATCAGTGCCAATATAGGATAGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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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 | |||
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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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FCAR - Fc fragment of IgA receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002000.3 | 451 | Missense Mutation | CAC,CGC | H,R 97 | NP_001991.1 | |
NM_133269.3 | 451 | Missense Mutation | CAC,CGC | H,R 97 | NP_579803.1 | |
NM_133271.3 | 451 | Missense Mutation | CAC,CGC | H,R 97 | NP_579805.1 | |
NM_133272.3 | 451 | Missense Mutation | CAC,CGC | H,R 85 | NP_579806.1 | |
NM_133273.3 | 451 | Missense Mutation | CAC,CGC | H,R 85 | NP_579807.1 | |
NM_133274.3 | 451 | Missense Mutation | CAC,CGC | H,R 85 | NP_579808.1 | |
NM_133277.3 | 451 | Intron | NP_579811.1 | |||
NM_133278.3 | 451 | Missense Mutation | CAC,CGC | H,R 85 | NP_579812.1 | |
XM_011526625.2 | 451 | Missense Mutation | CAC,CGC | H,R 70 | XP_011524927.1 | |
XM_017026473.1 | 451 | Missense Mutation | CAC,CGC | H,R 70 | XP_016881962.1 | |
XM_017026474.1 | 451 | Missense Mutation | CAC,CGC | H,R 70 | XP_016881963.1 |