Search Thermo Fisher Scientific
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GGACCCAGATTACCAGGAGGCGCTT[C/T]GCAGCCTGTGTCAGAAAAGAGACGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607113 | ||||||||||||||||||||
Literature Links: |
APOBEC3G 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 |
APOBEC3G - apolipoprotein B mRNA editing enzyme catalytic subunit 3G | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_021822.3 | 763 | Missense Mutation | CGC,TGC | R,C 136 | NP_068594.1 | |
XM_006724290.1 | 763 | Missense Mutation | CGC,TGC | R,C 69 | XP_006724353.1 | |
XM_017028903.1 | 763 | Missense Mutation | CGC,TGC | R,C 136 | XP_016884392.1 | |
XM_017028904.1 | 763 | Missense Mutation | CGC,TGC | R,C 69 | XP_016884393.1 |