BMP15 bone morphogenetic protein 15
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 14 |
Likely pathogenic | 0 | 6 |
Benign | 0 | 24 |
Likely benign | 0 | 18 |
Conflicting classifications of pathogenicity | 0 | 8 |
not provided | 6 | 0 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
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0 |
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0 |
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22 |
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58 |
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12 |
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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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 |
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Target data | : |
MGeND data only
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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 | GDF9B |
SYNONYM | ODG2 |
SYNONYM | POF4 |
MIM | 300247 OMIM |
HGNC | HGNC:1068 HGNC |
Ensembl | ENSG00000130385 Ensembl |
AllianceGenome | HGNC:1068 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000252677.4 | hg38 | chrX | 50,910,735 | 50,916,641 | 5,907 |
ENST00000252677.4 | hg19 | chrX | 50,653,735 | 50,659,641 | 5,907 |
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