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ACTAATGTCTTAGGACAAGCCCTCA[G/T]CCTCTATGACTTGGGCTATTCCAGT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
40 submissions
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Phenotype: |
MIM: 606891 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
FCRLA 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)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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FCRLA - Fc receptor like A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001184866.1 | Intron | NP_001171795.1 | ||||
NM_001184867.1 | Intron | NP_001171796.1 | ||||
NM_001184870.1 | Intron | NP_001171799.1 | ||||
NM_001184871.1 | Intron | NP_001171800.1 | ||||
NM_001184872.1 | Intron | NP_001171801.1 | ||||
NM_001184873.1 | Intron | NP_001171802.1 | ||||
NM_032738.3 | Intron | NP_116127.3 | ||||
XM_006711581.3 | Intron | XP_006711644.1 | ||||
XM_011510064.1 | Intron | XP_011508366.1 | ||||
XM_011510065.1 | Intron | XP_011508367.1 | ||||
XM_011510066.1 | Intron | XP_011508368.1 |
Set Membership: |
HapMap |