SPAG7 sperm associated antigen 7
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 6 |
Uncertain significance | 0 | 22 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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28 |
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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
[No Data.]
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 | ACRP |
SYNONYM | FSA-1 |
MIM | 610056 OMIM |
HGNC | HGNC:11216 HGNC |
Ensembl | ENSG00000091640 Ensembl |
AllianceGenome | HGNC:11216 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000206020.8 | hg38 | chr17 | 4,959,226 | 4,967,817 | 8,592 |
ENST00000573366.5 | hg38 | chr17 | 4,959,256 | 4,967,191 | 7,936 |
ENST00000575142.5 | hg38 | chr17 | 4,959,226 | 4,967,790 | 8,565 |
ENST00000575142.5 | hg19 | chr17 | 4,862,521 | 4,871,085 | 8,565 |
ENST00000206020.8 | hg19 | chr17 | 4,862,521 | 4,871,112 | 8,592 |
ENST00000573366.5 | hg19 | chr17 | 4,862,551 | 4,870,486 | 7,936 |
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