Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAAGCAGATTTTTATTCAGACTTCC[A/G]ATGGGCTTATCTTGTCCCCTCCAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 613362 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CINP 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
|
CINP - cyclin dependent kinase 2 interacting protein | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320046.1 | 2548 | Intron | NP_001306975.1 | |||
NM_032630.2 | 2548 | Intron | NP_116019.1 |
ZNF839 - zinc finger protein 839 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001267827.1 | 2548 | Missense Mutation | AAT,GAT | N,D 779 | NP_001254756.1 | |
NM_001267828.1 | 2548 | Missense Mutation | AAT,GAT | N,D 779 | NP_001254757.1 | |
NM_018335.4 | 2548 | Missense Mutation | AAT,GAT | N,D 895 | NP_060805.3 | |
XM_006720203.3 | 2548 | Missense Mutation | AAT,GAT | N,D 807 | XP_006720266.2 | |
XM_011536945.1 | 2548 | Missense Mutation | AAT,GAT | N,D 929 | XP_011535247.1 | |
XM_011536946.2 | 2548 | Missense Mutation | AAT,GAT | N,D 879 | XP_011535248.1 | |
XM_011536948.2 | 2548 | Missense Mutation | AAT,GAT | N,D 779 | XP_011535250.1 | |
XM_011536949.2 | 2548 | Intron | XP_011535251.1 | |||
XM_011536950.2 | 2548 | Intron | XP_011535252.1 | |||
XM_017021447.1 | 2548 | Missense Mutation | AAT,GAT | N,D 845 | XP_016876936.1 | |
XM_017021448.1 | 2548 | Intron | XP_016876937.1 | |||
XM_017021449.1 | 2548 | Missense Mutation | AAT,GAT | N,D 560 | XP_016876938.1 | |
XM_017021450.1 | 2548 | Intron | XP_016876939.1 | |||
XM_017021451.1 | 2548 | Intron | XP_016876940.1 |