GDF3 growth differentiation factor 3
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely pathogenic | 0 | 4 |
Benign | 4 | 26 |
Likely benign | 0 | 20 |
Conflicting classifications of pathogenicity | 0 | 2 |
Uncertain significance | 0 | 54 |
Ranking
ClinVar | |
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0 |
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0 |
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14 |
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86 |
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4 |
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 | KFS3 |
SYNONYM | MCOP7 |
SYNONYM | MCOPCB6 |
MIM | 606522 OMIM |
HGNC | HGNC:4218 HGNC |
Ensembl | ENSG00000184344 Ensembl |
AllianceGenome | HGNC:4218 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000329913.4 | hg38 | chr12 | 7,689,784 | 7,695,775 | 5,992 |
ENST00000329913.4 | hg19 | chr12 | 7,842,380 | 7,848,371 | 5,992 |
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