ENST00000327787.13 FAAP100
Information
- Transcript ID
- ENST00000327787.13
- Genome
- hg19
- Position
- chr17:79,506,917-79,519,379
- Strand
- -
- CDS length
- 2,646
- Amino acid length
- 882
- Gene symbol
- FAAP100
- Gene type
- protein-coding
- Gene description
- FA core complex associated protein 100
- Gene Entrez Gene ID
- 80233
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 |
|---|---|---|
| 9 | 79,506,917 | 79,507,976 |
| 8 | 79,508,335 | 79,508,421 |
| 7 | 79,511,030 | 79,511,146 |
| 6 | 79,512,772 | 79,512,908 |
| 5 | 79,513,935 | 79,514,704 |
| 4 | 79,516,232 | 79,516,388 |
| 3 | 79,517,274 | 79,518,229 |
| 2 | 79,518,954 | 79,519,078 |
| 1 | 79,519,192 | 79,519,379 |
CDS
| Exon number | Type | Start | Stop |
|---|---|---|---|
| 9 | CDS | 79,507,845 | 79,507,976 |
| 8 | CDS | 79,508,335 | 79,508,421 |
| 7 | CDS | 79,511,030 | 79,511,146 |
| 6 | CDS | 79,512,772 | 79,512,908 |
| 5 | CDS | 79,513,935 | 79,514,704 |
| 4 | CDS | 79,516,232 | 79,516,388 |
| 3 | CDS | 79,517,274 | 79,518,229 |
| 2 | CDS | 79,518,954 | 79,519,078 |
| 1 | CDS | 79,519,192 | 79,519,356 |
Other genome
| Genome | Chromosome | Start | End | Links |
|---|---|---|---|---|
| hg38 | chr17 | 81,539,891 | 81,552,353 | Link |
CDS sequence
ATGGCCGGCGCCGCGCCGCGGGTCCGCTACCTGGCGGGCTTCTGCTGCCCTCTCGGGGGCCTGGCGGCGGGCAAGCCCCGCGTGCTGTGCCATGAGGCAGAGGTCTTCCTGTCCACCGGGAGCGAGCTCGTCTACGTGTACGACCAGGAGGGCGGGCTGCTGACCGCGGCGTTCCGGTTCCCCGACCAGGTGTGGCACCTGGAGCTGCTGGCGCCGCGCAGGTTGCTGTACGCGCTGTGCGCCCGGAGGGGCCTCTACTGCCTGTCGCTGGACCACCCGGGCAGGAGCAGGTCTACGAGCCAGGATGACAGGGACAGCGAGGACGGTGACCAGCCTTCCCCCGTGATCCCTGTGGACCCCGATGCCTGCATCCTTCCCGATGCTGCGCTGTGCGCGTTCACCTTGCTGGACAGTGTGCTGGTCACCCTGGTGCAGGGCCCTGCCCGATGGAAGATGCAGCTGTTTGAGCAGCCCTGTCCTGGGGAGGACCCCCGGCCAGGAGGCCAGATCGGTGAGGTGGAGCTGTCCTCCTACACGCCCCCAGCCGGGGTCCCAGGAAAGCCTGCAGCCCCCCACTTCCTTCCAGTGCTGTGCTCTGTGTCACCATCAGGCTCCAGGGTCCCGCACGACCTCCTCGGGGGCTCCGGGGGCTTCACGCTGGAGGACGCCCTCTTCGGGCTCCTCTTTGGAGCTGATGCCACCCTCCTGCAGTCACCTGTGGTCCTCTGTGGTCTCCCTGATGGCCAGCTCTGCTGTGTGATCCTGAAGGCCCTGGTCACCTCCAGGTCAGCCCCTGGTGACCCAAATGCCCTTGTCAAGATCCTCCATCACCTGGAGGAGCCCGTCATCTTCATAGGGGCCTTGAAGACAGAGCCACAGGCTGCAGAAGCTGCAGAGAATTTTCTGCCTGACGAGGATGTGCACTGTGACTGCCTGGTGGCCTTTGGTCACCACGGCCGGATGCTGGCCATCAAGGCCAGCTGGGATGAGTCCGGGAAGCTGGTGCCCGAGCTGCGGGAGTACTGCCTCCCAGGCCCTGTGCTCTGCGCTGCCTGTGGCGGGGGTGGCCGCGTGTACCACAGCACCCCTTCTGACCTCTGTGTGGTGGATCTGTCTCGGGGAAGCACCCCGCTGGGCCCTGAGCAGCCCGAAGAAGGCCCGGGAGGCCTGCCCCCCATGCTGTGCCCAGCCAGCCTGAACATCTGCAGTGTCGTCTCGCTGTCCGCGTCTCCCAGGACGCATGAAGGTGGCACCAAGCTCCTGGCCCTGTCCGCCAAAGGCCGCCTGATGACCTGCAGCCTGGACCTGGACTCTGAGATGCCTGGCCCAGCCAGGATGACCACAGAGAGTGCAGGTCAGAAAATAAAGGAGCTGCTGTCTGGAATTGGCAACATCTCTGAGAGAGTGTCTTTTCTAAAGAAGGCGGTTGACCAGCGGAACAAGGCACTGACAAGCCTCAACGAGGCCATGAACGTGAGCTGTGCACTGCTGTCAAGCGGCACGGGCCCCAGACCCATCTCCTGCACCACCAGCACCACCTGGAGCCGCCTGCAGACACAGGATGTGCTCATGGCCACCTGCGTGCTAGAGAACAGCAGCAGCTTCAGCCTGGACCAGGGGTGGACCCTGTGCATCCAGGTGCTCACCAGCTCCTGTGCTCTCGACCTGGACTCGGCCTGCTCCGCCATCACCTACACCATCCCCGTGGACCAGCTCGGCCCCGGTGCTCGGCGGGAGGTGACGCTACCCCTGGGCCCTGGTGAGAACGGCGGGCTCGACCTGCCCGTGACCGTGTCCTGCACGCTGTTCTACAGTCTCAGGGAGGTGGTGGGCGGGGCCCTTGCCCCCTCAGACTCTGAGGACCCCTTTCTGGATGAGTGCCCCTCCGACGTCCTGCCCGAGCAAGAGGGTGTTTGCCTGCCCCTGAGCAGGCACACAGTGGACATGCTGCAGTGTCTGCGCTTCCCTGGCCTGGCCCCGCCACACACACGGGCCCCCTCCCCACTCGGCCCCACCCGAGACCCTGTGGCCACTTTTCTGGAAACTTGTCGGGAGCCTGGCAGCCAGCCAGCAGGACCCGCCTCCCTGCGGGCCGAGTACCTGCCCCCATCTGTGGCTTCCATCAAGGTGTCGGCGGAGCTGCTCAGAGCTGCCTTGAAGGACGGCCACTCAGGCGTGCCCCTGTGCTGTGCCACCCTGCAGTGGCTCCTTGCTGAGAATGCTGCTGTGGACGTCGTGAGGGCCCGAGCACTATCTTCCATCCAGGGAGTGGCCCCTGATGGCGCCAACGTTCACCTCATCGTCCGAGAGGTGGCCATGACTGACCTGTGCCCAGCAGGGCCCATCCAGGCCGTGGAGATTCAAGTGGAAAGCTCCTCTCTGGCCGACATTTGCAGGGCGCACCATGCCGTTGTCGGGCGCATGCAGACGATGGTGACAGAGCAGGCCACCCAGGGCTCCAGCGCTCCTGATCTCCGTGTGCAGTACCTCCGCCAGATCCACGCCAACCACGAGACACTGCTGCGGGAGGTGCAGACCCTGCGCGACCGGCTCTGCACGGAGGATGAGGCCAGCTCCTGTGCCACCGCCCAGAGGCTGCTACAGGTGTACCGGCAGCTGCGCCACCCCAGCCTCATCCTGCTGTGA
Amino sequence
MAGAAPRVRYLAGFCCPLGGLAAGKPRVLCHEAEVFLSTGSELVYVYDQEGGLLTAAFRFPDQVWHLELLAPRRLLYALCARRGLYCLSLDHPGRSRSTSQDDRDSEDGDQPSPVIPVDPDACILPDAALCAFTLLDSVLVTLVQGPARWKMQLFEQPCPGEDPRPGGQIGEVELSSYTPPAGVPGKPAAPHFLPVLCSVSPSGSRVPHDLLGGSGGFTLEDALFGLLFGADATLLQSPVVLCGLPDGQLCCVILKALVTSRSAPGDPNALVKILHHLEEPVIFIGALKTEPQAAEAAENFLPDEDVHCDCLVAFGHHGRMLAIKASWDESGKLVPELREYCLPGPVLCAACGGGGRVYHSTPSDLCVVDLSRGSTPLGPEQPEEGPGGLPPMLCPASLNICSVVSLSASPRTHEGGTKLLALSAKGRLMTCSLDLDSEMPGPARMTTESAGQKIKELLSGIGNISERVSFLKKAVDQRNKALTSLNEAMNVSCALLSSGTGPRPISCTTSTTWSRLQTQDVLMATCVLENSSSFSLDQGWTLCIQVLTSSCALDLDSACSAITYTIPVDQLGPGARREVTLPLGPGENGGLDLPVTVSCTLFYSLREVVGGALAPSDSEDPFLDECPSDVLPEQEGVCLPLSRHTVDMLQCLRFPGLAPPHTRAPSPLGPTRDPVATFLETCREPGSQPAGPASLRAEYLPPSVASIKVSAELLRAALKDGHSGVPLCCATLQWLLAENAAVDVVRARALSSIQGVAPDGANVHLIVREVAMTDLCPAGPIQAVEIQVESSSLADICRAHHAVVGRMQTMVTEQATQGSSAPDLRVQYLRQIHANHETLLREVQTLRDRLCTEDEASSCATAQRLLQVYRQLRHPSLILL*