Product Details
- SNP ID
-
rs199988578
- Assay Type
- Functionally Tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.19:14595314 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CTTCTCCATTGCAGCCATCCCTGGC[C/T]GGTAAGTGTCCTCCCATTTCCCCTC
- Phenotype
-
MIM: 606101
MIM: 616838
- Polymorphism
- C/T, Transition Substitution
- Allele Nomenclature
-
- Literature Links
-
ADGRE3
PubMed Links
- Additional Information
-
For this assay, SNP(s) [rs369612439] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Gene Details
- Gene
- ADGRE3
- Gene Name
- adhesion G protein-coupled receptor E3
There are no transcripts associated with this gene.
- Gene
- CLEC17A
- Gene Name
- C-type lectin domain family 17 member A
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001204118.1 |
1072 |
Silent Mutation |
GCC,GCT |
A148A |
NP_001191047.1 |
NM_207390.3 |
1072 |
Silent Mutation |
GCC,GCT |
A148A |
NP_997273.3 |
XM_017026785.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882274.1 |
XM_017026786.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882275.1 |
XM_017026787.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882276.1 |
XM_017026788.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882277.1 |
XM_017026789.1 |
1072 |
Intron |
|
|
XP_016882278.1 |
XM_017026790.1 |
1072 |
Silent Mutation |
GCC,GCT |
A63A |
XP_016882279.1 |
XM_017026791.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882280.1 |
XM_017026792.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882281.1 |
XM_017026793.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882282.1 |
XM_017026794.1 |
1072 |
Silent Mutation |
GCC,GCT |
A80A |
XP_016882283.1 |
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