FAAH fatty acid amide hydrolase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely pathogenic | 0 | 2 |
Benign | 0 | 24 |
Likely benign | 0 | 14 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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2 |
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84 |
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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
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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 |
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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 | |||
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Entry | Origin | Type | Annotation |
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | FAAH-1 |
SYNONYM | FAAH1 |
SYNONYM | PSAB |
MIM | 602935 OMIM |
HGNC | HGNC:3553 HGNC |
Ensembl | ENSG00000117480 Ensembl |
AllianceGenome | HGNC:3553 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000243167.9 | hg38 | chr1 | 46,394,317 | 46,413,845 | 19,529 |
ENST00000243167.9 | hg19 | chr1 | 46,859,989 | 46,879,517 | 19,529 |
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