ENST00000580212.6 CORO6
Information
- Transcript ID
- ENST00000580212.6
- Genome
- hg38
- Position
- chr17:29,614,765-29,622,912
- Strand
- -
- CDS length
- 1,299
- Amino acid length
- 433
- Gene symbol
- CORO6
- Gene type
- protein-coding
- Gene description
- coronin 6
- Gene Entrez Gene ID
- 84940
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 |
---|---|---|
10 | 29,614,765 | 29,615,857 |
9 | 29,615,945 | 29,616,175 |
8 | 29,616,279 | 29,616,336 |
7 | 29,616,702 | 29,616,847 |
6 | 29,616,938 | 29,617,042 |
5 | 29,618,790 | 29,618,971 |
4 | 29,619,060 | 29,619,189 |
3 | 29,619,651 | 29,619,773 |
2 | 29,621,224 | 29,621,484 |
1 | 29,622,688 | 29,622,912 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
10 | CDS | 29,615,732 | 29,615,857 |
9 | CDS | 29,615,945 | 29,616,175 |
8 | CDS | 29,616,279 | 29,616,336 |
7 | CDS | 29,616,702 | 29,616,847 |
6 | CDS | 29,616,938 | 29,617,042 |
5 | CDS | 29,618,790 | 29,618,971 |
4 | CDS | 29,619,060 | 29,619,189 |
3 | CDS | 29,619,651 | 29,619,773 |
2 | CDS | 29,621,224 | 29,621,421 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg19 | chr17 | 27,941,783 | 27,949,930 | Link |
CDS sequence
ATGAGCAGACGTGTGGTTCGGCAAAGCAAGTTCCGCCATGTGTTTGGGCAGGCAGCAAAGGCCGACCAGGCCTACGAGGACATCCGTGTGTCCAAGGTCACATGGGACAGCTCCTTCTGTGCCGTCAACCCCAAATTCCTGGCCATTATTGTGGAGGCTGGAGGCGGGGGTGCCTTCATCGTCCTGCCTCTGGCCAAGACAGGGCGAGTGGATAAGAACTACCCACTGGTCACTGGGCACACTGCCCCTGTGCTGGATATTGACTGGTGTCCACACAATGACAACGTTATCGCCAGTGCCTCAGACGACACCACCATCATGGTGTGGCAGATTCCAGACTATACCCCCATGCGCAACATTACGGAACCTATCATCACACTTGAGGGCCACTCCAAGCGTGTGGGCATCCTCTCCTGGCACCCTACTGCCAGGAATGTCCTGCTCAGTGCAGGTGGTGACAATGTGATCATCATCTGGAATGTGGGCACCGGGGAGGTGCTGCTGAGCCTGGATGATATGCACCCAGACGTCATCCACAGTGTGTGCTGGAACAGCAACGGTAGCCTGCTAGCCACCACCTGCAAGGACAAGACCTTGCGCATCATTGACCCCAGAAAAGGCCAAGTGGTGGCGAACAACTTCGAGGAGCCAGTGGCACTGCAGGAGATGGACACAAGCAACGGGGTCCTATTGCCCTTTTACGATCCCGACTCCAGCATCGTCTACCTGTGTGGCAAGGGCGACAGCAGCATTCGGTACTTTGAGATTACCGACGAGCCGCCTTTCGTGCACTACCTGAACACGTTCAGCAGCAAAGAGCCGCAGCGGGGCATGGGTTTCATGCCCAAAAGGGGACTGGATGTCAGCAAGTGTGAGATCGCCCGGTTCTACAAGCTACACGAAAGAAAGTGTGAACCTATCATCATGACTGTGCCCCGCAAGTCAGACCTCTTCCAGGACGATCTGTACCCGGATACGCCAGGCCCGGAGCCGGCCCTAGAAGCGGACGAATGGCTATCCGGCCAGGACGCCGAACCCGTGCTCATTTCGCTGAGGGACGGCTATGTGCCCCCCAAGCACCGCGAGCTCCGGGTCACGAAGCGCAACATCCTGGACGTGCGCCCGCCCTCCGGCCCCCGCCGCAGCCAGTCGGCCAGCGACGCCCCCTTGTCGCAGCAGCACACCCTGGAGACGCTGCTGGAAGAGATCAAGGCCCTCCGCGAGCGGGTGCAGGCCCAGGAGCAGCGCATCACGGCTCTGGAGAACATGCTGTGCGAGCTGGTGGACGGCACGGACTAG
Amino sequence
MSRRVVRQSKFRHVFGQAAKADQAYEDIRVSKVTWDSSFCAVNPKFLAIIVEAGGGGAFIVLPLAKTGRVDKNYPLVTGHTAPVLDIDWCPHNDNVIASASDDTTIMVWQIPDYTPMRNITEPIITLEGHSKRVGILSWHPTARNVLLSAGGDNVIIIWNVGTGEVLLSLDDMHPDVIHSVCWNSNGSLLATTCKDKTLRIIDPRKGQVVANNFEEPVALQEMDTSNGVLLPFYDPDSSIVYLCGKGDSSIRYFEITDEPPFVHYLNTFSSKEPQRGMGFMPKRGLDVSKCEIARFYKLHERKCEPIIMTVPRKSDLFQDDLYPDTPGPEPALEADEWLSGQDAEPVLISLRDGYVPPKHRELRVTKRNILDVRPPSGPRRSQSASDAPLSQQHTLETLLEEIKALRERVQAQEQRITALENMLCELVDGTD*