Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGCTGGGGGTTCCCAGCCGGCCCTC[C/T]GGAGCCGGGGGACTGCGACGGCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 186852 MIM: 608735 | ||||||||||||||||||||
Literature Links: |
MIR4487 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
MIR4487 - microRNA 4487 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
PSMC3 - proteasome 26S subunit, ATPase 3 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
SLC39A13 - solute carrier family 39 member 13 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001128225.2 | 167 | Missense Mutation | CGG,TGG | R,W 38 | NP_001121697.1 | |
NM_152264.4 | 167 | Missense Mutation | CGG,TGG | R,W 38 | NP_689477.2 | |
XM_006718381.3 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_006718444.1 | |
XM_006718383.3 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_006718446.1 | |
XM_006718384.2 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_006718447.1 | |
XM_006718385.2 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_006718448.1 | |
XM_011520466.1 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_011518768.1 | |
XM_011520467.1 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_011518769.1 | |
XM_011520468.2 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_011518770.1 | |
XM_011520469.1 | 167 | Missense Mutation | CGG,TGG | R,W 53 | XP_011518771.1 | |
XM_011520470.1 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_011518772.1 | |
XM_017018540.1 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_016874029.1 | |
XM_017018541.1 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_016874030.1 | |
XM_017018542.1 | 167 | Missense Mutation | CGG,TGG | R,W 38 | XP_016874031.1 |