Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGGCCCAGCGTCTACCGCAACGTGG[C/T]GCGTCAGCTGCACATCTCCCTGCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 605404 | ||||||||||||||||||||
Literature Links: |
BOK 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 |
BOK - BOK, BCL2 family apoptosis regulator | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032515.4 | 362 | Missense Mutation | GCG,GTG | A,V 89 | NP_115904.1 | |
XM_011511696.2 | 362 | Missense Mutation | GCG,GTG | A,V 89 | XP_011509998.1 | |
XM_011511697.2 | 362 | Missense Mutation | GCG,GTG | A,V 89 | XP_011509999.1 | |
XM_017004775.1 | 362 | Missense Mutation | GCG,GTG | A,V 11 | XP_016860264.1 | |
XM_017004776.1 | 362 | Missense Mutation | GCG,GTG | A,V 11 | XP_016860265.1 |
BOK-AS1 - BOK antisense RNA 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |