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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | EDF |
| SYNONYM | FRP |
| MIM | 147290 OMIM |
| HGNC | HGNC:6066 HGNC |
| Ensembl | ENSG00000122641 Ensembl |
| AllianceGenome | HGNC:6066 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| 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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