Product Details
- SNP ID
-
rs9073
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.10:50806851 on Build GRCh38
- Set Membership
-
HapMap
- Context Sequence [VIC/FAM]
- GCTTGCTTGAGCTGGGCTGCAGACA[C/T]GGGTGCAGTTGCATTAGGGACAGCA
- Phenotype
-
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
A1CF
PubMed Links
Gene Details
- Gene
- A1CF
- Gene Name
- APOBEC1 complementation factor
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001198818.1 |
1920 |
Missense Mutation |
ATG,GTG |
M547V |
NP_001185747.1 |
NM_001198819.1 |
1920 |
Missense Mutation |
ATG,GTG |
M563V |
NP_001185748.1 |
NM_001198820.1 |
1920 |
Missense Mutation |
ATG,GTG |
M555V |
NP_001185749.1 |
NM_014576.3 |
1920 |
Missense Mutation |
ATG,GTG |
M547V |
NP_055391.2 |
NM_138932.2 |
1920 |
Missense Mutation |
ATG,GTG |
M555V |
NP_620310.1 |
NM_138933.2 |
1920 |
Missense Mutation |
ATG,GTG |
M555V |
NP_620311.1 |
XM_005269718.2 |
1920 |
Missense Mutation |
ATG,GTG |
M555V |
XP_005269775.1 |
XM_005269720.3 |
1920 |
Missense Mutation |
ATG,GTG |
M555V |
XP_005269777.1 |
XM_011539729.2 |
1920 |
Missense Mutation |
ATG,GTG |
M563V |
XP_011538031.1 |
XM_011539730.2 |
1920 |
Missense Mutation |
ATG,GTG |
M508V |
XP_011538032.1 |
XM_017016160.1 |
1920 |
Missense Mutation |
ATG,GTG |
M547V |
XP_016871649.1 |
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