ENST00000397536.7 CCDC9B
Information
- Transcript ID
- ENST00000397536.7
- Genome
- hg19
- Position
- chr15:40,623,653-40,633,140
- Strand
- -
- CDS length
- 1,473
- Amino acid length
- 491
- Gene symbol
- CCDC9B
- Gene type
- protein-coding
- Gene description
- coiled-coil domain containing 9B
- Gene Entrez Gene ID
- 388115
Variants
Display target variant
Search Word
Target data | : |
MGeND data only
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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 |
---|---|---|
11 | 40,623,653 | 40,627,901 |
10 | 40,627,985 | 40,628,027 |
9 | 40,628,775 | 40,628,865 |
8 | 40,628,961 | 40,629,014 |
7 | 40,629,589 | 40,629,647 |
6 | 40,629,925 | 40,630,094 |
5 | 40,630,736 | 40,630,861 |
4 | 40,630,949 | 40,631,104 |
3 | 40,631,713 | 40,631,820 |
2 | 40,632,106 | 40,632,216 |
1 | 40,633,009 | 40,633,140 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
11 | CDS | 40,627,359 | 40,627,901 |
10 | CDS | 40,627,985 | 40,628,027 |
9 | CDS | 40,628,775 | 40,628,865 |
8 | CDS | 40,628,961 | 40,629,014 |
7 | CDS | 40,629,589 | 40,629,647 |
6 | CDS | 40,629,925 | 40,630,094 |
5 | CDS | 40,630,736 | 40,630,861 |
4 | CDS | 40,630,949 | 40,631,104 |
3 | CDS | 40,631,713 | 40,631,820 |
2 | CDS | 40,632,106 | 40,632,216 |
1 | CDS | 40,633,009 | 40,633,020 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr15 | 40,331,452 | 40,340,939 | Link |
CDS sequence
ATGCACTCGGCTGGAACTCCCAGAGCCGAGTCCCCCATGAGCAGGCAGGAGAAGGACGCAGAGCTGGATCGGAGGATAGTTGCCCTGCGCAAGAAGAACCAGGCCTTGCTCCGCAGGTACCAGGAGATCCAGGAGGACCGTCGGCAGGCAGAGCAGGGGGGGATGGCTGTGACCACACCAGCACTCCTCCAGCCTGATGGCCTCACCGTTACCATCAGCCAGGTTCCCGGTGAAAAGCGGGTGGTTAGCAGGAACTGGGCAAGGGGTACCTGTGGACCCAGAGTGACCAACGAGATGCTTGAGGATGAGGATGCTGAGGACCACGGGGGTACTTTCTGCTTAGGGGAGCTGGTGGAGCTGGCTGTGACCATGGAGAACAAAGCAGAGGGCAAACGGATTGTAAGTGAAAAGCCTACCAGAGCAAGGAACCAAGGCATAGAGGGGTCACCTGGAGGGCGTGTGACCCGAAGCCCCCCCACGCAGGTGGCCATCAGCTCAGATTCTGCACGGAAGGGTTCTTGGGAGCCCTGGAGCCGGCCGGTGGGGGAGCCCCCGGAGGCGGGCTGGGACTATGCCCAGTGGAAGCAGGAGCGGGAGCAGATCGACCTAGCCCGCCTCGCCCGGCACAGAGACGCACAGGGTGACTGGCGCCGCCCGTGGGACCTGGACAAGGCCAAGTCCACGCTACAGGACTGCAGCCAGCTGAGGGGAGAAGGCCCGGCCAGGGCAGGCAGCAGAAGGGGTCCCAGGAGCCACCAGAAACTACAGCCCCCACCATTGCTCCCTGATGGAAAAGGTCGGGGCGGGCAAGCCAGCAGACCCTCGGTGGCACCAGCCACAGGCAGCAAAGCCCGGGGCAAGGAGAGGCTGACTGGCAGGGCCCGAAGGTGGGATATGAAGGAAGACAAGGAGGAGCTGGAAGGTCAGGAGGGAAGCCAAAGCACCAGAGAGACTCCCAGTGAGGAGGAGCAAGCCCAGAAGCAGAGCGGGATGGAGCAGGGCCGACTGGGGAGCGCCCCTGCAGCCAGCCCAGCCCTGGCATCCCCAGAGGGGCCGAAGGGGGAGTCAGTGGCTTCCACAGCCAGCTCAGTCCCCTGCTCTCCACAGGAGCCTGACTTGGCTCCTCTTGACCTCTCCCTAGGAGGGGCTGGCATCCCTGGGCCCAGGGAGAGCGGGTGTGTGCTCGGTCTGAGGCCTGGGGCCCAGGAGAGCCCTGTGTCTTGGCCAGAGGGCTCTAAGCAGCAGCCCCTGGGGTGGAGCAATCACCAGGCTGAGCTGGAAGTACAGACTTGCCCTGAGCCACAGAGAGGAGCAGGGCTCCCAGAGCCCGGAGAAGACAGGTCTGGCAAGTCTGGGGCCCAGCAGGGCCTGGCCCCGAGAAGCCGGCCCACGAGAGGAGGCAGCCAAAGGTCGAGAGGCACAGCAGGTGTGAGGCGCAGGACAGGGCGCCCTGGCCCGGCAGGAAGATGCTGA
Amino sequence
MHSAGTPRAESPMSRQEKDAELDRRIVALRKKNQALLRRYQEIQEDRRQAEQGGMAVTTPALLQPDGLTVTISQVPGEKRVVSRNWARGTCGPRVTNEMLEDEDAEDHGGTFCLGELVELAVTMENKAEGKRIVSEKPTRARNQGIEGSPGGRVTRSPPTQVAISSDSARKGSWEPWSRPVGEPPEAGWDYAQWKQEREQIDLARLARHRDAQGDWRRPWDLDKAKSTLQDCSQLRGEGPARAGSRRGPRSHQKLQPPPLLPDGKGRGGQASRPSVAPATGSKARGKERLTGRARRWDMKEDKEELEGQEGSQSTRETPSEEEQAQKQSGMEQGRLGSAPAASPALASPEGPKGESVASTASSVPCSPQEPDLAPLDLSLGGAGIPGPRESGCVLGLRPGAQESPVSWPEGSKQQPLGWSNHQAELEVQTCPEPQRGAGLPEPGEDRSGKSGAQQGLAPRSRPTRGGSQRSRGTAGVRRRTGRPGPAGRC*