ENST00000610417.5 SAMD4B
Information
- Transcript ID
- ENST00000610417.5
- Genome
- hg38
- Position
- chr19:39,342,421-39,385,700
- Strand
- +
- CDS length
- 2,085
- Amino acid length
- 695
- Gene symbol
- SAMD4B
- Gene type
- protein-coding
- Gene description
- sterile alpha motif domain containing 4B
- Gene Entrez Gene ID
- 55095
Variants
Display target variant
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| 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 | 39,342,421 | 39,342,576 |
| 2 | 39,354,006 | 39,354,066 |
| 3 | 39,356,689 | 39,357,089 |
| 4 | 39,369,655 | 39,370,125 |
| 5 | 39,375,650 | 39,375,889 |
| 6 | 39,376,437 | 39,376,546 |
| 7 | 39,376,705 | 39,376,791 |
| 8 | 39,377,485 | 39,377,824 |
| 9 | 39,378,504 | 39,378,589 |
| 10 | 39,379,966 | 39,380,084 |
| 11 | 39,380,587 | 39,380,785 |
| 12 | 39,380,990 | 39,381,113 |
| 13 | 39,383,208 | 39,383,291 |
| 14 | 39,383,499 | 39,385,700 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 3 | CDS | 39,356,894 | 39,357,089 |
| 4 | CDS | 39,369,655 | 39,370,125 |
| 5 | CDS | 39,375,650 | 39,375,889 |
| 6 | CDS | 39,376,437 | 39,376,546 |
| 7 | CDS | 39,376,705 | 39,376,791 |
| 8 | CDS | 39,377,485 | 39,377,824 |
| 9 | CDS | 39,378,504 | 39,378,589 |
| 10 | CDS | 39,379,966 | 39,380,084 |
| 11 | CDS | 39,380,587 | 39,380,785 |
| 12 | CDS | 39,380,990 | 39,381,113 |
| 13 | CDS | 39,383,208 | 39,383,291 |
| 14 | CDS | 39,383,499 | 39,383,527 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg19 | chr19 | 39,833,061 | 39,876,340 | Link |
CDS sequence
ATGATGTTCCGAGACCAGGTGGGCATCCTCGCTGGCTGGTTCAAAGGCTGGAATGAGTGTGAGCAGACAGTGGCCCTCCTGTCACTTCTGAAACGGGTCACCCGTACCCAGGCCCGCTTCCTGCAGCTCTGCCTGGAGCACTCACTGGCGGACTGCAATGACATCCACCTGCTGGAGTCGGAGGCCAACAGTGCTGCCATCGTCAGCCAGTGGCAGCAGGAGTCCAAAGAGAAGGTGGTGTCCCTCCTGCTGTCCCACCTTCCCCTGCTTCAGCCAGGCAACACAGAGGCCAAGTCGGAGTACATGAGGCTACTGCAGAAAGTGCTGGCCTACTCAATCGAGAGCAATGCTTTCATCGAGGAGAGTCGCCAGCTGCTTTCCTATGCCCTCATCCACCCAGCCACCACACTGGAGGACCGCAACGCACTGGCCCTCTGGCTGAGCCACCTGGAAGAGCGGTTGGCTAGTGGCTTCCGCTCCCGGCCAGAGCCCTCCTACCATTCACGTCAAGGCTCAGATGAGTGGGGGGGCCCTGCAGAGCTAGGCCCTGGGGAGGCAGGGCCAGGCTGGCAGGACAAGCCACCCCGGGAAAATGGACACGTGCCCTTCCACCCATCCAGCTCAGTGCCGCCAGCCATCAACAGTATTGGGAGCAATGCAAACACAGGTCTCCCCTGCCAAATCCACCCTAGCCCACTGAAGCGCTCCATGTCACTCATCCCTACAAGCCCCCAGGTCCCTGGTGAGTGGCCGAGTCCAGAGGAGCTTGGGGCCCGGGCTGCTTTTACCACGCCCGATCACGCACCTCTCTCGCCCCAGAGCAGCGTGGCCTCCTCTGGCAGTGAGCAGACAGAGGAGCAGGGCTCCAGCCGGAACACCTTCCAGGAGGATGGCAGTGGCATGAAAGATGTGCCCTCATGGCTCAAGAGCCTCCGTTTGCACAAGTATGCAGCCCTCTTCTCACAGATGAGCTACGAGGAGATGATGACACTGACTGAGCAGCACCTGGAGTCTCAGAACGTCACCAAAGGTGCCCGCCACAAGATAGCCCTGAGCATCCAGAAGCTGCGTGAGAGACAGAGCGTCCTCAAGTCCCTAGAGAAGGATGTGCTGGAAGGCGGGAACCTACGAAACGCTCTGCAGGAGCTGCAGCAGATCATCATCACTCCCATCAAGGCCTACAGTGTCCTCCAGGCCACCGTGGCTGCCGCCACCACCACCCCTACTGCCAAGGATGGGGCCCCGGGGGAACCACCGCTGCCAGGTGCTGAGCCTCCCCTAGCCCACCCCGGCACAGACAAAGGCACCGAGGCCAAGGACCCTCCAGCTGTGGAGAACTACCCACCTCCACCAGCTCCAGCTCCCACTGATGGCAGTGAGCCTGCCCCGGCTCCCGTCGCCGACGGAGACATCCCCAGCCAGTTTACACGGGTGATGGGCAAAGTGTGCACCCAACTGCTGGTGTCCCGACCAGACGAGGAGAACATCACCAGTTACCTCCAGCTCATCGAAAAGTGCCTGACTCATGAGGCTTTCACGGAGACGCAGAAGAAACGGCTGCTATCCTGGAAACAGCAAGTGCTGAAGCTCCTCCGGACATTCCCGCGCAAAGCCGCACTAGAGATGCAGAACTACCGGCAGCAGAAAGGCTGGGCATTCGGCTCCAACTCGCTCCCCATAGCTGGCTCTGTGGGGATGGGAGTGGCCCGGCGTACCCAGCGGCAGTTCCCAATGCCTCCCCGGGCCCTCCCACCCGGCCGGATGGGCCTCCTGAGCCCCTCGGGCATTGGGGGTGTCTCCCCTCGACATGCCCTCACCAGCCCCAGCCTTGGAGGCCAGGGCCGACAGAACCTGTGGTTTGCCAACCCTGGAGGCAGCAACAGCATGCCCAGTCAGAGCCGCAGCTCTGTGCAGCGCACCCACTCGCTCCCGGTCCACTCGTCACCCCAGGCCATTCTCATGTTCCCTCCAGACTGCCCGGTTCCTGGGCCTGACCTGGAGATCAATCCCACTCTGGAGTCTCTGTGTCTGAGCATGACAGAACACGCCTTGGGTGATGGGACAGACAAAACCTCCACCATCTGA
Amino sequence
MMFRDQVGILAGWFKGWNECEQTVALLSLLKRVTRTQARFLQLCLEHSLADCNDIHLLESEANSAAIVSQWQQESKEKVVSLLLSHLPLLQPGNTEAKSEYMRLLQKVLAYSIESNAFIEESRQLLSYALIHPATTLEDRNALALWLSHLEERLASGFRSRPEPSYHSRQGSDEWGGPAELGPGEAGPGWQDKPPRENGHVPFHPSSSVPPAINSIGSNANTGLPCQIHPSPLKRSMSLIPTSPQVPGEWPSPEELGARAAFTTPDHAPLSPQSSVASSGSEQTEEQGSSRNTFQEDGSGMKDVPSWLKSLRLHKYAALFSQMSYEEMMTLTEQHLESQNVTKGARHKIALSIQKLRERQSVLKSLEKDVLEGGNLRNALQELQQIIITPIKAYSVLQATVAAATTTPTAKDGAPGEPPLPGAEPPLAHPGTDKGTEAKDPPAVENYPPPPAPAPTDGSEPAPAPVADGDIPSQFTRVMGKVCTQLLVSRPDEENITSYLQLIEKCLTHEAFTETQKKRLLSWKQQVLKLLRTFPRKAALEMQNYRQQKGWAFGSNSLPIAGSVGMGVARRTQRQFPMPPRALPPGRMGLLSPSGIGGVSPRHALTSPSLGGQGRQNLWFANPGGSNSMPSQSRSSVQRTHSLPVHSSPQAILMFPPDCPVPGPDLEINPTLESLCLSMTEHALGDGTDKTSTI*