GLMN glomulin, FKBP associated protein
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 38 |
Likely pathogenic | 0 | 34 |
Benign | 6 | 76 |
Likely benign | 0 | 14 |
Conflicting classifications of pathogenicity | 0 | 10 |
Uncertain significance | 0 | 58 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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36 |
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168 |
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2 |
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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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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Target data | : |
MGeND data only
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | FAP |
SYNONYM | FAP48 |
SYNONYM | FAP68 |
SYNONYM | FKBPAP |
SYNONYM | GLML |
SYNONYM | GVM |
SYNONYM | VMGLOM |
MIM | 601749 OMIM |
HGNC | HGNC:14373 HGNC |
Ensembl | ENSG00000174842 Ensembl |
AllianceGenome | HGNC:14373 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000370360.8 | hg38 | chr1 | 92,246,402 | 92,298,987 | 52,586 |
ENST00000370360.8 | hg19 | chr1 | 92,711,959 | 92,764,544 | 52,586 |
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