FAM118B family with sequence similarity 118 member B
Information
- Symbol
- FAM118B
- Type
- protein-coding
- Description
- family with sequence similarity 118 member B
- Entrez Gene ID
- 79607
- Genome
- hg19
- Position
- chr11:126,081,677-126,132,863
- Genome
- hg38
- Position
- chr11:126,211,782-126,262,968
- MIM
- 616587 OMIM
- HGNC
- HGNC:26110 HGNC
- Ensembl
- ENSG00000197798 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 34 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
36 |
 |
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
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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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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| 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
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| Category | : |
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| 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 |
|---|---|
| MIM | 616587 OMIM |
| HGNC | HGNC:26110 HGNC |
| Ensembl | ENSG00000197798 Ensembl |
| AllianceGenome | HGNC:26110 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000627851.2 | hg38 | chr11 | 126,211,724 | 126,262,984 | 51,261 |
| ENST00000533050.6 | hg38 | chr11 | 126,211,782 | 126,262,968 | 51,187 |
| ENST00000529731.5 | hg38 | chr11 | 126,211,773 | 126,262,268 | 50,496 |
| ENST00000360194.8 | hg38 | chr11 | 126,211,773 | 126,262,631 | 50,859 |
| ENST00000627851.2 | hg19 | chr11 | 126,081,619 | 126,132,879 | 51,261 |
| ENST00000529731.5 | hg19 | chr11 | 126,081,668 | 126,132,163 | 50,496 |
| ENST00000360194.8 | hg19 | chr11 | 126,081,668 | 126,132,526 | 50,859 |
| ENST00000533050.6 | hg19 | chr11 | 126,081,677 | 126,132,863 | 51,187 |
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