INHBA inhibin subunit beta A
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 11 | 2 |
Uncertain significance | 0 | 24 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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24 |
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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
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 | |||||
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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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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 | EDF |
SYNONYM | FRP |
MIM | 147290 OMIM |
HGNC | HGNC:6066 HGNC |
Ensembl | ENSG00000122641 Ensembl |
AllianceGenome | HGNC:6066 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000638023.1 | hg38 | chr7 | 41,689,590 | 41,705,834 | 16,245 |
ENST00000242208.5 | hg38 | chr7 | 41,685,114 | 41,703,090 | 17,977 |
ENST00000442711.1 | hg38 | chr7 | 41,689,534 | 41,700,609 | 11,076 |
ENST00000242208.5 | hg19 | chr7 | 41,724,712 | 41,742,688 | 17,977 |
ENST00000442711.1 | hg19 | chr7 | 41,729,132 | 41,740,207 | 11,076 |
ENST00000638023.1 | hg19 | chr7 | 41,729,188 | 41,745,432 | 16,245 |
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