ENST00000392672.8 RAD9B
Information
- Transcript ID
- ENST00000392672.8
- Genome
- hg38
- Position
- chr12:110,502,239-110,532,086
- Strand
- +
- CDS length
- 1,290
- Amino acid length
- 430
- Gene symbol
- RAD9B
- Gene type
- protein-coding
- Gene description
- RAD9 checkpoint clamp component B
- Gene Entrez Gene ID
- 144715
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
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| Search word | : | |
| Filtering | : |
| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
Exon
| Exon number | Start | Stop |
|---|---|---|
| 1 | 110,502,239 | 110,502,383 |
| 2 | 110,503,806 | 110,503,876 |
| 3 | 110,505,617 | 110,505,772 |
| 4 | 110,506,579 | 110,506,693 |
| 5 | 110,512,779 | 110,512,878 |
| 6 | 110,515,050 | 110,515,156 |
| 7 | 110,518,676 | 110,518,782 |
| 8 | 110,518,874 | 110,518,938 |
| 9 | 110,519,794 | 110,519,916 |
| 10 | 110,522,177 | 110,522,411 |
| 11 | 110,530,525 | 110,530,633 |
| 12 | 110,531,574 | 110,532,086 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 1 | CDS | 110,502,338 | 110,502,383 |
| 2 | CDS | 110,503,806 | 110,503,876 |
| 3 | CDS | 110,505,617 | 110,505,772 |
| 4 | CDS | 110,506,579 | 110,506,693 |
| 5 | CDS | 110,512,779 | 110,512,878 |
| 6 | CDS | 110,515,050 | 110,515,156 |
| 7 | CDS | 110,518,676 | 110,518,782 |
| 8 | CDS | 110,518,874 | 110,518,938 |
| 9 | CDS | 110,519,794 | 110,519,916 |
| 10 | CDS | 110,522,177 | 110,522,411 |
| 11 | CDS | 110,530,525 | 110,530,633 |
| 12 | CDS | 110,531,574 | 110,531,629 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr12 | 110,940,044 | 110,969,891 | Link |
CDS sequence
ATGGCAGCCATGCTGAAGTGCGTGATGAGCGGCAGTCAGGTGAAAGTATTTGGGAAAGCAGTTCAAGCTCTATCACGAATTAGTGACGAGTTCTGGCTAGACCCATCTAAAAAAGGTCTTGCTCTAAGATGTGTGAATTCTTCTCGGTCAGCATATGGATGTGTCCTGTTCTCTCCTGTGTTTTTTCAGCATTATCAATGGTCAGCTTTAGTGAAAATGAGTGAAAATGAACTTGACACAACACTGCATTTAAAATGCAAATTGGGAATGAAGTCAATTTTGCCCATCTTTAGATGTCTGAATTCCCTTGAAAGAAATATAGAGAAGTGCAGAATATTCACCAGATCTGATAAATGCAAAGTAGTTATTCAATTCTTCTACAGACATGGTATTAAAAGAACTCATAATATATGTTTTCAAGAAAGTCAGCCTTTGCAAGTTATTTTTGACAAGAATGTTTGTACTAATACGCTAATGATTCAACCAAGATTGCTTGCTGATGCCATTGTTCTTTTTACATCAAGTCAAGAGGAAGTTACTCTTGCTGTTACTCCACTGAATTTTTGCCTCAAGAGTTCTAATGAGGAATCAATGGATTTGAGCAATGCTGTACACAGTGAGATGTTTGTTGGCTCAGATGAGTTTGACTTCTTTCAAATTGGAATGGACACTGAGATAACATTTTGTTTCAAAGAATTGAAGGGAATACTGACATTTTCAGAAGCTACACATGCTCCTATATCCATTTATTTTGATTTCCCTGGGAAACCTCTGGCTTTGAGTATTGATGATATGTTAGTGGAAGCTAACTTTATTTTGGCCACATTAGCTGATGAACAAAGTAGAGCATCTTCACCACAGTCACTGTGTCTTTCACAGAAACGAAAAAGGTCAGATCTGATTGAAAAAAAGGCTGGCAAAAATGTAACTGGCCAGGCCCTGGAATGTATTTCAAAAAAAGCAGCACCAAGAAGGCTTTATCCTAAGGAGACTCTCACAAACATATCTGCATTGGAAAACTGTGGCAGCCCTGCAATGAAAAGAGTGGATGGAGATGTCAGTGAAGTATCAGAAAGCAGTGTCAGCAACACAGAGGAAGTGCCAGGGTCTCTGTGTCTCAGAAAGTTTTCTTGCATGTTCTTTGGAGCAGTTTCTTCTGACCAGCAAGAACACTTCAACCACCCTTTCGACAGTCTGGCAAGAGCAAGTGACAGTGAAGAGGACATGAATAATGTGTGCTGCAGGAAAGAATTTAATGGAAGTGATGCCAAATATTTCTGTATTATCTGA
Amino sequence
MAAMLKCVMSGSQVKVFGKAVQALSRISDEFWLDPSKKGLALRCVNSSRSAYGCVLFSPVFFQHYQWSALVKMSENELDTTLHLKCKLGMKSILPIFRCLNSLERNIEKCRIFTRSDKCKVVIQFFYRHGIKRTHNICFQESQPLQVIFDKNVCTNTLMIQPRLLADAIVLFTSSQEEVTLAVTPLNFCLKSSNEESMDLSNAVHSEMFVGSDEFDFFQIGMDTEITFCFKELKGILTFSEATHAPISIYFDFPGKPLALSIDDMLVEANFILATLADEQSRASSPQSLCLSQKRKRSDLIEKKAGKNVTGQALECISKKAAPRRLYPKETLTNISALENCGSPAMKRVDGDVSEVSESSVSNTEEVPGSLCLRKFSCMFFGAVSSDQQEHFNHPFDSLARASDSEEDMNNVCCRKEFNGSDAKYFCII*