Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 612041 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RNF212 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
|
RNF212 - ring finger protein 212 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001131034.3 | 430 | Intron | NP_001124506.1 | |||
NM_001193318.2 | 430 | Intron | NP_001180247.1 | |||
NM_194439.4 | 430 | Intron | NP_919420.1 | |||
XM_005272274.2 | 430 | Missense Mutation | XP_005272331.1 | |||
XM_011513439.1 | 430 | Intron | XP_011511741.1 | |||
XM_011513443.1 | 430 | Intron | XP_011511745.1 | |||
XM_011513444.1 | 430 | Missense Mutation | XP_011511746.1 | |||
XM_011513445.2 | 430 | Intron | XP_011511747.1 | |||
XM_011513446.1 | 430 | Missense Mutation | XP_011511748.1 | |||
XM_017008039.1 | 430 | Intron | XP_016863528.1 | |||
XM_017008040.1 | 430 | Intron | XP_016863529.1 | |||
XM_017008041.1 | 430 | Intron | XP_016863530.1 | |||
XM_017008042.1 | 430 | Intron | XP_016863531.1 |