Product Details
- SNP ID
-
rs202247225
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.12:30710328 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GCTGAGGCAGAGGGTAGACGTGTAC[C/T]GGCAGTATGGTGGCTGCTGGATTTG
- Phenotype
-
MIM: 610375
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
CAPRIN2
PubMed Links
Gene Details
- Gene
- CAPRIN2
- Gene Name
- caprin family member 2
| Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
| NM_001002259.2 |
2885 |
Silent Mutation |
CCA,CCG |
P986P |
NP_001002259.1 |
| NM_001206856.2 |
2885 |
UTR 3 |
|
|
NP_001193785.1 |
| NM_001319842.1 |
2885 |
Silent Mutation |
CCA,CCG |
P652P |
NP_001306771.1 |
| NM_001319843.1 |
2885 |
Silent Mutation |
CCA,CCG |
P985P |
NP_001306772.1 |
| NM_001319844.1 |
2885 |
Silent Mutation |
CCA,CCG |
P870P |
NP_001306773.1 |
| NM_001319845.1 |
2885 |
Silent Mutation |
CCA,CCG |
P905P |
NP_001306774.1 |
| NM_001319846.1 |
2885 |
Silent Mutation |
CCA,CCG |
P905P |
NP_001306775.1 |
| NM_023925.4 |
2885 |
Silent Mutation |
CCA,CCG |
P936P |
NP_076414.2 |
| NM_032156.4 |
2885 |
UTR 3 |
|
|
NP_115532.3 |
| XM_006719138.3 |
2885 |
Silent Mutation |
CCA,CCG |
P965P |
XP_006719201.1 |
| XM_006719139.3 |
2885 |
Silent Mutation |
CCA,CCG |
P951P |
XP_006719202.1 |
| XM_006719140.3 |
2885 |
Silent Mutation |
CCA,CCG |
P950P |
XP_006719203.1 |
| XM_006719142.3 |
2885 |
Silent Mutation |
CCA,CCG |
P916P |
XP_006719205.1 |
| XM_006719144.3 |
2885 |
Silent Mutation |
CCA,CCG |
P902P |
XP_006719207.1 |
| XM_006719145.3 |
2885 |
UTR 3 |
|
|
XP_006719208.1 |
| XM_006719146.3 |
2885 |
UTR 3 |
|
|
XP_006719209.1 |
| XM_006719147.3 |
2885 |
UTR 3 |
|
|
XP_006719210.1 |
| XM_017019851.1 |
2885 |
Silent Mutation |
CCA,CCG |
P930P |
XP_016875340.1 |
| XM_017019852.1 |
2885 |
Silent Mutation |
CCA,CCG |
P904P |
XP_016875341.1 |
| XM_017019853.1 |
2885 |
Silent Mutation |
CCA,CCG |
P904P |
XP_016875342.1 |
| XM_017019854.1 |
2885 |
Silent Mutation |
CCA,CCG |
P901P |
XP_016875343.1 |
| XM_017019855.1 |
2885 |
Silent Mutation |
CCA,CCG |
P884P |
XP_016875344.1 |
| XM_017019856.1 |
2885 |
Silent Mutation |
CCA,CCG |
P870P |
XP_016875345.1 |
| XM_017019857.1 |
2885 |
Silent Mutation |
CCA,CCG |
P869P |
XP_016875346.1 |
| XM_017019858.1 |
2885 |
Silent Mutation |
CCA,CCG |
P869P |
XP_016875347.1 |
| XM_017019859.1 |
2885 |
Silent Mutation |
CCA,CCG |
P821P |
XP_016875348.1 |
| XM_017019860.1 |
2885 |
UTR 3 |
|
|
XP_016875349.1 |
| XM_017019861.1 |
2885 |
Silent Mutation |
CCA,CCG |
P820P |
XP_016875350.1 |
| XM_017019862.1 |
2885 |
UTR 3 |
|
|
XP_016875351.1 |
| XM_017019863.1 |
2885 |
UTR 3 |
|
|
XP_016875352.1 |
| XM_017019864.1 |
2885 |
Intron |
|
|
XP_016875353.1 |
| XM_017019865.1 |
2885 |
UTR 3 |
|
|
XP_016875354.1 |
| XM_017019866.1 |
2885 |
UTR 3 |
|
|
XP_016875355.1 |
| XM_017019867.1 |
2885 |
UTR 3 |
|
|
XP_016875356.1 |
| XM_017019868.1 |
2885 |
UTR 3 |
|
|
XP_016875357.1 |
| XM_017019869.1 |
2885 |
UTR 3 |
|
|
XP_016875358.1 |
| XM_017019870.1 |
2885 |
UTR 3 |
|
|
XP_016875359.1 |
| XM_017019871.1 |
2885 |
UTR 3 |
|
|
XP_016875360.1 |
| XM_017019872.1 |
2885 |
UTR 3 |
|
|
XP_016875361.1 |
| XM_017019873.1 |
2885 |
UTR 3 |
|
|
XP_016875362.1 |
| XM_017019874.1 |
2885 |
Silent Mutation |
CCA,CCG |
P652P |
XP_016875363.1 |
| XM_017019875.1 |
2885 |
UTR 3 |
|
|
XP_016875364.1 |
| XM_017019876.1 |
2885 |
Silent Mutation |
CCA,CCG |
P632P |
XP_016875365.1 |
| XM_017019877.1 |
2885 |
Silent Mutation |
CCA,CCG |
P618P |
XP_016875366.1 |
| XM_017019878.1 |
2885 |
Silent Mutation |
CCA,CCG |
P617P |
XP_016875367.1 |
| XM_017019879.1 |
2885 |
Silent Mutation |
CCA,CCG |
P597P |
XP_016875368.1 |
| XM_017019880.1 |
2885 |
Silent Mutation |
CCA,CCG |
P548P |
XP_016875369.1 |
| XM_017019881.1 |
2885 |
UTR 3 |
|
|
XP_016875370.1 |
| XM_017019882.1 |
2885 |
UTR 3 |
|
|
XP_016875371.1 |
| XM_017019883.1 |
2885 |
UTR 3 |
|
|
XP_016875372.1 |
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