Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
A1CF 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)
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SAS
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Chinese - Not Available | CHB (Han Chinese)
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AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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A1CF - APOBEC1 complementation factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198818.1 | 1920 | Missense Mutation | ATG,GTG | M,V 547 | NP_001185747.1 | |
NM_001198819.1 | 1920 | Missense Mutation | ATG,GTG | M,V 563 | NP_001185748.1 | |
NM_001198820.1 | 1920 | Missense Mutation | ATG,GTG | M,V 555 | NP_001185749.1 | |
NM_014576.3 | 1920 | Missense Mutation | ATG,GTG | M,V 547 | NP_055391.2 | |
NM_138932.2 | 1920 | Missense Mutation | ATG,GTG | M,V 555 | NP_620310.1 | |
NM_138933.2 | 1920 | Missense Mutation | ATG,GTG | M,V 555 | NP_620311.1 | |
XM_005269718.2 | 1920 | Missense Mutation | ATG,GTG | M,V 555 | XP_005269775.1 | |
XM_005269720.3 | 1920 | Missense Mutation | ATG,GTG | M,V 555 | XP_005269777.1 | |
XM_011539729.2 | 1920 | Missense Mutation | ATG,GTG | M,V 563 | XP_011538031.1 | |
XM_011539730.2 | 1920 | Missense Mutation | ATG,GTG | M,V 508 | XP_011538032.1 | |
XM_017016160.1 | 1920 | Missense Mutation | ATG,GTG | M,V 547 | XP_016871649.1 |
Set Membership: |
HapMap |