Product Details
- SNP ID
-
rs145705724
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.14:69054464 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GTGCTCATGGCCTGGGCCATTGCTG[A/G]GAGTTCTAGGAGTCTCTTCTTTAAA
- Phenotype
-
MIM: 603812
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
DCAF5
PubMed Links
Gene Details
- Gene
- DCAF5
- Gene Name
- DDB1 and CUL4 associated factor 5
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001284206.1 |
2438 |
Missense Mutation |
CCC,CTC |
P740L |
NP_001271135.1 |
NM_001284207.1 |
2438 |
Missense Mutation |
CCC,CTC |
P659L |
NP_001271136.1 |
NM_001284208.1 |
2438 |
Intron |
|
|
NP_001271137.1 |
NM_003861.2 |
2438 |
Missense Mutation |
CCC,CTC |
P741L |
NP_003852.1 |
XM_006720297.2 |
2438 |
Missense Mutation |
CCC,CTC |
P776L |
XP_006720360.1 |
XM_006720298.2 |
2438 |
Missense Mutation |
CCC,CTC |
P775L |
XP_006720361.1 |
XM_006720299.3 |
2438 |
Missense Mutation |
CCC,CTC |
P694L |
XP_006720362.1 |
XM_006720300.2 |
2438 |
Missense Mutation |
CCC,CTC |
P693L |
XP_006720363.1 |
XM_011537278.1 |
2438 |
Missense Mutation |
CCC,CTC |
P694L |
XP_011535580.1 |
XM_011537279.2 |
2438 |
Missense Mutation |
CCC,CTC |
P694L |
XP_011535581.1 |
XM_011537280.2 |
2438 |
Missense Mutation |
CCC,CTC |
P559L |
XP_011535582.1 |
XM_017021733.1 |
2438 |
Missense Mutation |
CCC,CTC |
P694L |
XP_016877222.1 |
XM_017021734.1 |
2438 |
Missense Mutation |
CCC,CTC |
P659L |
XP_016877223.1 |
XM_017021735.1 |
2438 |
Missense Mutation |
CCC,CTC |
P659L |
XP_016877224.1 |
XM_017021736.1 |
2438 |
Missense Mutation |
CCC,CTC |
P658L |
XP_016877225.1 |
XM_017021737.1 |
2438 |
Missense Mutation |
CCC,CTC |
P524L |
XP_016877226.1 |
XM_017021738.1 |
2438 |
Missense Mutation |
CCC,CTC |
P462L |
XP_016877227.1 |
XM_017021739.1 |
2438 |
Missense Mutation |
CCC,CTC |
P462L |
XP_016877228.1 |
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