Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAGGGAGGATGAAGAGGGGCTATTT[A/G]ATTCGCTGGGGGTCTTCCTGTCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
|||||||||||||||||||||||||||||||||||||||
Literature Links: |
C4orf51 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
|
C4orf51 - chromosome 4 open reading frame 51 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080531.1 | 3487 | Intron | NP_001074000.1 | |||
XM_006714289.3 | 3487 | Intron | XP_006714352.1 | |||
XM_011532196.2 | 3487 | Intron | XP_011530498.1 | |||
XM_011532197.2 | 3487 | Intron | XP_011530499.1 | |||
XM_017008547.1 | 3487 | Intron | XP_016864036.1 | |||
XM_017008548.1 | 3487 | Intron | XP_016864037.1 | |||
XM_017008549.1 | 3487 | Intron | XP_016864038.1 | |||
XM_017008550.1 | 3487 | Intron | XP_016864039.1 | |||
XM_017008551.1 | 3487 | Intron | XP_016864040.1 | |||
XM_017008552.1 | 3487 | Intron | XP_016864041.1 | |||
XM_017008553.1 | 3487 | Intron | XP_016864042.1 | |||
XM_017008554.1 | 3487 | Intron | XP_016864043.1 | |||
XM_017008555.1 | 3487 | Intron | XP_016864044.1 | |||
XM_017008556.1 | 3487 | Intron | XP_016864045.1 |
ZNF827 - zinc finger protein 827 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001306215.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | NP_001293144.1 | |
NM_178835.4 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | NP_849157.2 | |
XM_011531634.2 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_011529936.1 | |
XM_011531635.2 | 3487 | Missense Mutation | TCA,TTA | S,L 951 | XP_011529937.1 | |
XM_011531645.2 | 3487 | Missense Mutation | TCA,TTA | S,L 295 | XP_011529947.1 | |
XM_017007768.1 | 3487 | Missense Mutation | TCA,TTA | S,L 961 | XP_016863257.1 | |
XM_017007769.1 | 3487 | Missense Mutation | TCA,TTA | S,L 951 | XP_016863258.1 | |
XM_017007770.1 | 3487 | Missense Mutation | TCA,TTA | S,L 885 | XP_016863259.1 | |
XM_017007771.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_016863260.1 | |
XM_017007772.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_016863261.1 | |
XM_017007773.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_016863262.1 | |
XM_017007774.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_016863263.1 | |
XM_017007775.1 | 3487 | Missense Mutation | TCA,TTA | S,L 963 | XP_016863264.1 | |
XM_017007776.1 | 3487 | Intron | XP_016863265.1 | |||
XM_017007777.1 | 3487 | Missense Mutation | TCA,TTA | S,L 374 | XP_016863266.1 |