Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGGAGAATTCGCACAACCACGGGGA[C/T]GGTGCAGAGGACTTCAAGCAGCAGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 607777 | ||||||||||||||||||||
Literature Links: |
SIN3B 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 |
SIN3B - SIN3 transcription regulator family member B | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001297595.1 | 439 | Silent Mutation | GAC,GAT | D,D 135 | NP_001284524.1 | |
NM_001297597.1 | 439 | Intron | NP_001284526.1 | |||
NM_015260.3 | 439 | Silent Mutation | GAC,GAT | D,D 135 | NP_056075.1 | |
XM_006722704.1 | 439 | Intron | XP_006722767.1 |