ENST00000295049.9 RFTN2
Information
- Transcript ID
- ENST00000295049.9
- Genome
- hg19
- Position
- chr2:198,432,948-198,540,311
- Strand
- -
- CDS length
- 1,506
- Amino acid length
- 502
- Gene symbol
- RFTN2
- Gene type
- protein-coding
- Gene description
- raftlin family member 2
- Gene Entrez Gene ID
- 130132
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 |
---|---|---|
9 | 198,432,948 | 198,437,004 |
8 | 198,460,715 | 198,460,793 |
7 | 198,480,600 | 198,480,703 |
6 | 198,482,524 | 198,482,645 |
5 | 198,495,735 | 198,495,944 |
4 | 198,498,442 | 198,498,721 |
3 | 198,508,882 | 198,508,996 |
2 | 198,511,207 | 198,511,390 |
1 | 198,540,044 | 198,540,311 |
CDS
Exon number | Type | Start | Stop |
---|---|---|---|
9 | CDS | 198,436,732 | 198,437,004 |
8 | CDS | 198,460,715 | 198,460,793 |
7 | CDS | 198,480,600 | 198,480,703 |
6 | CDS | 198,482,524 | 198,482,645 |
5 | CDS | 198,495,735 | 198,495,944 |
4 | CDS | 198,498,442 | 198,498,721 |
3 | CDS | 198,508,882 | 198,508,996 |
2 | CDS | 198,511,207 | 198,511,390 |
1 | CDS | 198,540,044 | 198,540,182 |
Other genome
Genome | Chromosome | Start | End | Links |
---|---|---|---|---|
hg38 | chr2 | 197,568,224 | 197,675,587 | Link |
CDS sequence
ATGGGGTGCGGACTTAGAAAGCTAGAAGACCCTGATGATAGCAGCCCTGGAAAAATATTTTCTACCCTGAAGAGACCGCAAGTGGAAACAAAGACAGAATTTGCTTACGAATATGTATTGCTGGATTTTACTCTACAAGCTTCATCAAACCCAGAAGTCATCAAGATAAATTCAATTCTGGATATAGTAACAAAAGTGGAAAACTATTATCTTAAAGGATATATTGTCGGGGCTATTCATCCTGTTATACAACCTGTGGGGCAGCGAAAACACCTACCTGCAAGTTACCTATACAGAGTGGTGCTATTGCGCTTGAAATTAAGCCCAAAGAATTCGGCAGCACCCAGTGGACAAAGACGCCCAAGGCTCGTGATTGAGGAATGTCCCCTAACTTCTGAGGCACAAACAAATGACGCAGCAAAAGAACTGATAGAAAAGATTAATGTCGCTGCTAAAAGAGGAATGAAATTTGTTGGATTCATATCACAGCATTATTCTCCATCTAAATTCTGCAATGGAACCAACCATGATGGAGATATAGAATCGATGCTACATGTGAGACACGGTTCAGATGAAAACTGTAGAAGTTGGAATGAAGGGACGTTAAGTGGGCAGTCATCTGAAAGCGGAATTGAGGAAGAACTTCATCATGAAAGTGGACAGTATCAAATGGAACAAAATGGCAGCCCTACTTCCTCTAAATCAAGAAAGGGAGAAGCCTCAGATAACAAATTGTATACAGTCTTCAATGCTTTTGATGATGATTCAACCTCCTGGGCCTATCAGGAAGGCATCCTGTCAATGAAAGTAACAAGAAAAGGATCAGTCATTAGTACACTTGATGCTGATTGGCTGGAGTTAACTACCTTTTATTATAAACAAGGCTTGTCTTTAATTGATTCTTTTGTATTCTGGGAAACATCTAAAGGGGAACATTTGCCTAAATCTTTGGAAGGATTTTTTATCTATGAAGAAGAAGGTTCTGGAGTTCCAGGTTCTAGTAGGAAAGGAAATGATGCCATCGTAGTAGAACAATGGACTGTTATTGAGGGATGTGAAATCAAAACAGATTATGGCCCTCTGCTGCACACTCTGGCTGAATTCGGATGGCTTCTGACAAGCGTGTTGCCCACACCTGTATTGAGACATGACAGTGAAGGGAATTTGGCTACAAAGCAGATCGTATTCCTTCAGAGGCCAGTTATGTGGAATTCAGCTGCTCAAACACCAGATAAGAAAGCCAGCCGCCACATAAAAGGTGAAGACAAGAATAAAGCCACTAGTAGAAGCATCGGATTAGACACAACCTCGTCACAACCTGCAGAGAGCAGACACCTGCCTGAGGAGTGCCGCCTTTCTCCCTCCCGGGAATGCTGGACAAAGGAGGGAAGGCTGGCACAGCACAACAGCTTCTCTGGGTTCAGCAGCAGTGACAACGTCCTCCGGGAATTAGACGACGGACAGTTTGATCAGGAAGATGGAGTGACTCAGGTCACTTGTATGTGA
Amino sequence
MGCGLRKLEDPDDSSPGKIFSTLKRPQVETKTEFAYEYVLLDFTLQASSNPEVIKINSILDIVTKVENYYLKGYIVGAIHPVIQPVGQRKHLPASYLYRVVLLRLKLSPKNSAAPSGQRRPRLVIEECPLTSEAQTNDAAKELIEKINVAAKRGMKFVGFISQHYSPSKFCNGTNHDGDIESMLHVRHGSDENCRSWNEGTLSGQSSESGIEEELHHESGQYQMEQNGSPTSSKSRKGEASDNKLYTVFNAFDDDSTSWAYQEGILSMKVTRKGSVISTLDADWLELTTFYYKQGLSLIDSFVFWETSKGEHLPKSLEGFFIYEEEGSGVPGSSRKGNDAIVVEQWTVIEGCEIKTDYGPLLHTLAEFGWLLTSVLPTPVLRHDSEGNLATKQIVFLQRPVMWNSAAQTPDKKASRHIKGEDKNKATSRSIGLDTTSSQPAESRHLPEECRLSPSRECWTKEGRLAQHNSFSGFSSSDNVLRELDDGQFDQEDGVTQVTCM*