MOSPD3 motile sperm domain containing 3
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 26 |
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
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 |
Search Word
Target data | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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 | CDS3 |
SYNONYM | NET30 |
MIM | 609125 OMIM |
HGNC | HGNC:25078 HGNC |
Ensembl | ENSG00000106330 Ensembl |
AllianceGenome | HGNC:25078 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000424091.2 | hg38 | chr7 | 100,612,556 | 100,615,384 | 2,829 |
ENST00000379527.6 | hg38 | chr7 | 100,612,430 | 100,615,373 | 2,944 |
ENST00000393950.7 | hg38 | chr7 | 100,612,540 | 100,615,377 | 2,838 |
ENST00000223054.8 | hg38 | chr7 | 100,612,102 | 100,615,326 | 3,225 |
ENST00000223054.8 | hg19 | chr7 | 100,209,725 | 100,212,949 | 3,225 |
ENST00000379527.6 | hg19 | chr7 | 100,210,053 | 100,212,996 | 2,944 |
ENST00000393950.7 | hg19 | chr7 | 100,210,163 | 100,213,000 | 2,838 |
ENST00000424091.2 | hg19 | chr7 | 100,210,179 | 100,213,007 | 2,829 |
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