FAM219B family with sequence similarity 219 member B
Information
- Symbol
- FAM219B
- Type
- protein-coding
- Description
- family with sequence similarity 219 member B
- Entrez Gene ID
- 57184
- Genome
- hg19
- Position
- chr15:75,192,333-75,199,192
- Genome
- hg38
- Position
- chr15:74,899,992-74,906,851
- HGNC
- HGNC:24695 HGNC
- Ensembl
- ENSG00000178761 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 4 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 38 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
42 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| 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
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| Category | : |
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | C15orf17 |
| HGNC | HGNC:24695 HGNC |
| Ensembl | ENSG00000178761 Ensembl |
| AllianceGenome | HGNC:24695 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000563119.5 | hg38 | chr15 | 74,899,992 | 74,906,837 | 6,846 |
| ENST00000565772.5 | hg38 | chr15 | 74,902,001 | 74,906,613 | 4,613 |
| ENST00000357635.10 | hg38 | chr15 | 74,899,992 | 74,906,851 | 6,860 |
| ENST00000563119.5 | hg19 | chr15 | 75,192,333 | 75,199,178 | 6,846 |
| ENST00000357635.10 | hg19 | chr15 | 75,192,333 | 75,199,192 | 6,860 |
| ENST00000565772.5 | hg19 | chr15 | 75,194,342 | 75,198,954 | 4,613 |
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