Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
|||||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 612047 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
E2F8 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)
|
||||||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
|
||||||||
AMR
|
E2F8 - E2F transcription factor 8 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001256371.1 | 2542 | Missense Mutation | ATT,GTT | I,V 674 | NP_001243300.1 | |
NM_001256372.1 | 2542 | Missense Mutation | ATT,GTT | I,V 674 | NP_001243301.1 | |
NM_024680.3 | 2542 | Missense Mutation | ATT,GTT | I,V 674 | NP_078956.2 | |
XM_011520367.1 | 2542 | Missense Mutation | ATT,GTT | I,V 569 | XP_011518669.1 |
Set Membership: |
HapMap |