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- SNP ID:
- rs201802333
- Gene
-
CAPRIN2 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.12: 30711604 - 30711604 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
TCGTGGACCACCAGATGTCCCTCCT[C/T]GCTTATAACACTGCTGGAAATTATC
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610375
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Literature Links: |
CAPRIN2 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 |
| CAPRIN2 - caprin family member 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001002259.2 | 2660 | Missense Mutation | CAA,CGA | Q,R 926 | NP_001002259.1 | |
| NM_001206856.2 | 2660 | Missense Mutation | CAA,CGA | Q,R 870 | NP_001193785.1 | |
| NM_001319842.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 592 | NP_001306771.1 | |
| NM_001319843.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 925 | NP_001306772.1 | |
| NM_001319844.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 810 | NP_001306773.1 | |
| NM_001319845.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 845 | NP_001306774.1 | |
| NM_001319846.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 845 | NP_001306775.1 | |
| NM_023925.4 | 2660 | Missense Mutation | CAA,CGA | Q,R 876 | NP_076414.2 | |
| NM_032156.4 | 2660 | Missense Mutation | CAA,CGA | Q,R 925 | NP_115532.3 | |
| XM_006719138.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 905 | XP_006719201.1 | |
| XM_006719139.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 891 | XP_006719202.1 | |
| XM_006719140.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 890 | XP_006719203.1 | |
| XM_006719142.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 856 | XP_006719205.1 | |
| XM_006719144.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 842 | XP_006719207.1 | |
| XM_006719145.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 926 | XP_006719208.1 | |
| XM_006719146.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 926 | XP_006719209.1 | |
| XM_006719147.3 | 2660 | Missense Mutation | CAA,CGA | Q,R 905 | XP_006719210.1 | |
| XM_017019851.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 870 | XP_016875340.1 | |
| XM_017019852.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 844 | XP_016875341.1 | |
| XM_017019853.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 844 | XP_016875342.1 | |
| XM_017019854.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 841 | XP_016875343.1 | |
| XM_017019855.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 824 | XP_016875344.1 | |
| XM_017019856.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 810 | XP_016875345.1 | |
| XM_017019857.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 809 | XP_016875346.1 | |
| XM_017019858.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 809 | XP_016875347.1 | |
| XM_017019859.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 761 | XP_016875348.1 | |
| XM_017019860.1 | 2660 | Missense Mutation | AAG,GAG | K,E 941 | XP_016875349.1 | |
| XM_017019861.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 760 | XP_016875350.1 | |
| XM_017019862.1 | 2660 | Missense Mutation | AAG,GAG | K,E 940 | XP_016875351.1 | |
| XM_017019863.1 | 2660 | Missense Mutation | AAG,GAG | K,E 941 | XP_016875352.1 | |
| XM_017019864.1 | 2660 | Missense Mutation | AAG,GAG | K,E 941 | XP_016875353.1 | |
| XM_017019865.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 891 | XP_016875354.1 | |
| XM_017019866.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 845 | XP_016875355.1 | |
| XM_017019867.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 845 | XP_016875356.1 | |
| XM_017019868.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 844 | XP_016875357.1 | |
| XM_017019869.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 844 | XP_016875358.1 | |
| XM_017019870.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 824 | XP_016875359.1 | |
| XM_017019871.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 824 | XP_016875360.1 | |
| XM_017019872.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 789 | XP_016875361.1 | |
| XM_017019873.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 761 | XP_016875362.1 | |
| XM_017019874.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 592 | XP_016875363.1 | |
| XM_017019875.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 740 | XP_016875364.1 | |
| XM_017019876.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 572 | XP_016875365.1 | |
| XM_017019877.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 558 | XP_016875366.1 | |
| XM_017019878.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 557 | XP_016875367.1 | |
| XM_017019879.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 537 | XP_016875368.1 | |
| XM_017019880.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 488 | XP_016875369.1 | |
| XM_017019881.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 592 | XP_016875370.1 | |
| XM_017019882.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 572 | XP_016875371.1 | |
| XM_017019883.1 | 2660 | Missense Mutation | CAA,CGA | Q,R 558 | XP_016875372.1 | |
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