FAR2 fatty acyl-CoA reductase 2
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 48 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
52 |
 |
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
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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 | |||||||||||
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| 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 | : |
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| 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 | HEL-S-81 |
| SYNONYM | MLSTD1 |
| SYNONYM | SDR10E2 |
| MIM | 616156 OMIM |
| HGNC | HGNC:25531 HGNC |
| Ensembl | ENSG00000064763 Ensembl |
| AllianceGenome | HGNC:25531 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000690162.1 | hg38 | chr12 | 29,149,082 | 29,335,633 | 186,552 |
| ENST00000551451.6 | hg38 | chr12 | 29,149,135 | 29,331,370 | 182,236 |
| ENST00000551193.2 | hg38 | chr12 | 29,149,103 | 29,335,582 | 186,480 |
| ENST00000182377.8 | hg38 | chr12 | 29,223,665 | 29,334,073 | 110,409 |
| ENST00000536681.8 | hg38 | chr12 | 29,149,278 | 29,335,616 | 186,339 |
| ENST00000547759.2 | hg38 | chr12 | 29,149,135 | 29,335,569 | 186,435 |
| ENST00000547116.5 | hg38 | chr12 | 29,223,745 | 29,334,072 | 110,328 |
| ENST00000686419.1 | hg38 | chr12 | 29,149,133 | 29,341,121 | 191,989 |
| ENST00000182377.8 | hg19 | chr12 | 29,376,598 | 29,487,006 | 110,409 |
| ENST00000536681.8 | hg19 | chr12 | 29,302,211 | 29,488,549 | 186,339 |
| ENST00000547116.5 | hg19 | chr12 | 29,376,678 | 29,487,005 | 110,328 |
| ENST00000547759.2 | hg19 | chr12 | 29,302,068 | 29,488,502 | 186,435 |
| ENST00000551193.2 | hg19 | chr12 | 29,302,036 | 29,488,515 | 186,480 |
| ENST00000551451.6 | hg19 | chr12 | 29,302,068 | 29,484,303 | 182,236 |
| ENST00000686419.1 | hg19 | chr12 | 29,302,066 | 29,494,054 | 191,989 |
| ENST00000690162.1 | hg19 | chr12 | 29,302,015 | 29,488,566 | 186,552 |
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