Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAATTTGCTCGTGGACCACCAGATG[A/T]CCCTCCTCGCTTATAACACTGCTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 610375 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CAPRIN2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
CAPRIN2 - caprin family member 2 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001002259.2 | 2668 | Missense Mutation | ACA,TCA | T,S 929 | NP_001002259.1 | |
NM_001206856.2 | 2668 | Missense Mutation | ACA,TCA | T,S 873 | NP_001193785.1 | |
NM_001319842.1 | 2668 | Missense Mutation | ACA,TCA | T,S 595 | NP_001306771.1 | |
NM_001319843.1 | 2668 | Missense Mutation | ACA,TCA | T,S 928 | NP_001306772.1 | |
NM_001319844.1 | 2668 | Missense Mutation | ACA,TCA | T,S 813 | NP_001306773.1 | |
NM_001319845.1 | 2668 | Missense Mutation | ACA,TCA | T,S 848 | NP_001306774.1 | |
NM_001319846.1 | 2668 | Missense Mutation | ACA,TCA | T,S 848 | NP_001306775.1 | |
NM_023925.4 | 2668 | Missense Mutation | ACA,TCA | T,S 879 | NP_076414.2 | |
NM_032156.4 | 2668 | Missense Mutation | ACA,TCA | T,S 928 | NP_115532.3 | |
XM_006719138.3 | 2668 | Missense Mutation | ACA,TCA | T,S 908 | XP_006719201.1 | |
XM_006719139.3 | 2668 | Missense Mutation | ACA,TCA | T,S 894 | XP_006719202.1 | |
XM_006719140.3 | 2668 | Missense Mutation | ACA,TCA | T,S 893 | XP_006719203.1 | |
XM_006719142.3 | 2668 | Missense Mutation | ACA,TCA | T,S 859 | XP_006719205.1 | |
XM_006719144.3 | 2668 | Missense Mutation | ACA,TCA | T,S 845 | XP_006719207.1 | |
XM_006719145.3 | 2668 | Missense Mutation | ACA,TCA | T,S 929 | XP_006719208.1 | |
XM_006719146.3 | 2668 | Missense Mutation | ACA,TCA | T,S 929 | XP_006719209.1 | |
XM_006719147.3 | 2668 | Missense Mutation | ACA,TCA | T,S 908 | XP_006719210.1 | |
XM_017019851.1 | 2668 | Missense Mutation | ACA,TCA | T,S 873 | XP_016875340.1 | |
XM_017019852.1 | 2668 | Missense Mutation | ACA,TCA | T,S 847 | XP_016875341.1 | |
XM_017019853.1 | 2668 | Missense Mutation | ACA,TCA | T,S 847 | XP_016875342.1 | |
XM_017019854.1 | 2668 | Missense Mutation | ACA,TCA | T,S 844 | XP_016875343.1 | |
XM_017019855.1 | 2668 | Missense Mutation | ACA,TCA | T,S 827 | XP_016875344.1 | |
XM_017019856.1 | 2668 | Missense Mutation | ACA,TCA | T,S 813 | XP_016875345.1 | |
XM_017019857.1 | 2668 | Missense Mutation | ACA,TCA | T,S 812 | XP_016875346.1 | |
XM_017019858.1 | 2668 | Missense Mutation | ACA,TCA | T,S 812 | XP_016875347.1 | |
XM_017019859.1 | 2668 | Missense Mutation | ACA,TCA | T,S 764 | XP_016875348.1 | |
XM_017019860.1 | 2668 | Silent Mutation | GGA,GGT | G,G 943 | XP_016875349.1 | |
XM_017019861.1 | 2668 | Missense Mutation | ACA,TCA | T,S 763 | XP_016875350.1 | |
XM_017019862.1 | 2668 | Silent Mutation | GGA,GGT | G,G 942 | XP_016875351.1 | |
XM_017019863.1 | 2668 | Silent Mutation | GGA,GGT | G,G 943 | XP_016875352.1 | |
XM_017019864.1 | 2668 | Silent Mutation | GGA,GGT | G,G 943 | XP_016875353.1 | |
XM_017019865.1 | 2668 | Missense Mutation | ACA,TCA | T,S 894 | XP_016875354.1 | |
XM_017019866.1 | 2668 | Missense Mutation | ACA,TCA | T,S 848 | XP_016875355.1 | |
XM_017019867.1 | 2668 | Missense Mutation | ACA,TCA | T,S 848 | XP_016875356.1 | |
XM_017019868.1 | 2668 | Missense Mutation | ACA,TCA | T,S 847 | XP_016875357.1 | |
XM_017019869.1 | 2668 | Missense Mutation | ACA,TCA | T,S 847 | XP_016875358.1 | |
XM_017019870.1 | 2668 | Missense Mutation | ACA,TCA | T,S 827 | XP_016875359.1 | |
XM_017019871.1 | 2668 | Missense Mutation | ACA,TCA | T,S 827 | XP_016875360.1 | |
XM_017019872.1 | 2668 | Missense Mutation | ACA,TCA | T,S 792 | XP_016875361.1 | |
XM_017019873.1 | 2668 | Missense Mutation | ACA,TCA | T,S 764 | XP_016875362.1 | |
XM_017019874.1 | 2668 | Missense Mutation | ACA,TCA | T,S 595 | XP_016875363.1 | |
XM_017019875.1 | 2668 | Missense Mutation | ACA,TCA | T,S 743 | XP_016875364.1 | |
XM_017019876.1 | 2668 | Missense Mutation | ACA,TCA | T,S 575 | XP_016875365.1 | |
XM_017019877.1 | 2668 | Missense Mutation | ACA,TCA | T,S 561 | XP_016875366.1 | |
XM_017019878.1 | 2668 | Missense Mutation | ACA,TCA | T,S 560 | XP_016875367.1 | |
XM_017019879.1 | 2668 | Missense Mutation | ACA,TCA | T,S 540 | XP_016875368.1 | |
XM_017019880.1 | 2668 | Missense Mutation | ACA,TCA | T,S 491 | XP_016875369.1 | |
XM_017019881.1 | 2668 | Missense Mutation | ACA,TCA | T,S 595 | XP_016875370.1 | |
XM_017019882.1 | 2668 | Missense Mutation | ACA,TCA | T,S 575 | XP_016875371.1 | |
XM_017019883.1 | 2668 | Missense Mutation | ACA,TCA | T,S 561 | XP_016875372.1 |