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ATAAGCATAAACAGGGCCAGCATGG[C/T]AGAGACAGGAGCCAGGGTCCGAGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
26 submissions
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Phenotype: |
MIM: 605484 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FCAMR 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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FCAMR - Fc fragment of IgA and IgM receptor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001122979.2 | 1714 | Silent Mutation | CTA,CTG | L,L 234 | NP_001116451.1 | |
NM_001170631.1 | 1714 | Missense Mutation | ACC,GCC | T,A 502 | NP_001164102.1 | |
NM_032029.4 | 1714 | Silent Mutation | CTA,CTG | L,L 234 | NP_114418.2 | |
XM_011510051.2 | 1714 | Missense Mutation | ACC,GCC | T,A 502 | XP_011508353.1 | |
XM_011510052.2 | 1714 | Missense Mutation | ACC,GCC | T,A 490 | XP_011508354.1 | |
XM_017002442.1 | 1714 | Missense Mutation | ACC,GCC | T,A 502 | XP_016857931.1 |