Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGTCATGCGAACTGAACCCAGTTCT[C/T]GATTAATCCTTTCCAAACGATCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 605501 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MPHOSPH9 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
|
MPHOSPH9 - M-phase phosphoprotein 9 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_022782.3 | 3744 | Missense Mutation | CAA,CGA | Q,R 1162 | NP_073619.3 | |
XM_011537740.2 | 3744 | Intron | XP_011536042.1 | |||
XM_011537741.2 | 3744 | Intron | XP_011536043.1 | |||
XM_017018673.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1162 | XP_016874162.1 | |
XM_017018674.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1128 | XP_016874163.1 | |
XM_017018675.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1120 | XP_016874164.1 | |
XM_017018676.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1110 | XP_016874165.1 | |
XM_017018677.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1087 | XP_016874166.1 | |
XM_017018678.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1053 | XP_016874167.1 | |
XM_017018679.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1010 | XP_016874168.1 | |
XM_017018680.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 1010 | XP_016874169.1 | |
XM_017018681.1 | 3744 | Missense Mutation | CAA,CGA | Q,R 789 | XP_016874170.1 |