Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCCCCGGCGCGGAGCAGACCGCCG[A/G]CAGCCTCCTCTACACCACGCCGCAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 600427 | ||||||||||||||||||||
Literature Links: |
E2F3 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 |
E2F3 - E2F transcription factor 3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001243076.2 | 984 | Intron | NP_001230005.1 | |||
NM_001949.4 | 984 | Missense Mutation | GAC,GGC | D,G 96 | NP_001940.1 | |
XM_005248865.4 | 984 | Intron | XP_005248922.1 | |||
XM_005248866.4 | 984 | Intron | XP_005248923.1 | |||
XM_011514324.2 | 984 | Missense Mutation | GAC,GGC | D,G 96 | XP_011512626.1 | |
XM_011514328.2 | 984 | Intron | XP_011512630.1 | |||
XM_017010330.1 | 984 | Intron | XP_016865819.1 |