TMPRSS4 transmembrane serine protease 4
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 12 |
Uncertain significance | 0 | 42 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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54 |
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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 | CAP2 |
SYNONYM | CAPH2 |
SYNONYM | MT-SP2 |
SYNONYM | TMPRSS3 |
MIM | 606565 OMIM |
HGNC | HGNC:11878 HGNC |
Ensembl | ENSG00000137648 Ensembl |
AllianceGenome | HGNC:11878 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000616579.4 | hg38 | chr11 | 118,077,012 | 118,119,839 | 42,828 |
ENST00000522151.6 | hg38 | chr11 | 118,077,130 | 118,118,155 | 41,026 |
ENST00000522824.5 | hg38 | chr11 | 118,077,094 | 118,118,457 | 41,364 |
ENST00000437212.8 | hg38 | chr11 | 118,077,078 | 118,121,890 | 44,813 |
ENST00000534111.5 | hg38 | chr11 | 118,077,038 | 118,121,890 | 44,853 |
ENST00000517544.2 | hg38 | chr11 | 118,077,015 | 118,108,223 | 31,209 |
ENST00000522307.5 | hg38 | chr11 | 118,077,076 | 118,118,091 | 41,016 |
ENST00000523251.5 | hg38 | chr11 | 118,077,077 | 118,118,182 | 41,106 |
ENST00000517544.2 | hg19 | chr11 | 117,947,730 | 117,978,938 | 31,209 |
ENST00000437212.8 | hg19 | chr11 | 117,947,793 | 117,992,605 | 44,813 |
ENST00000522151.6 | hg19 | chr11 | 117,947,845 | 117,988,870 | 41,026 |
ENST00000522824.5 | hg19 | chr11 | 117,947,809 | 117,989,172 | 41,364 |
ENST00000522307.5 | hg19 | chr11 | 117,947,791 | 117,988,806 | 41,016 |
ENST00000523251.5 | hg19 | chr11 | 117,947,792 | 117,988,897 | 41,106 |
ENST00000616579.4 | hg19 | chr11 | 117,947,727 | 117,990,554 | 42,828 |
ENST00000534111.5 | hg19 | chr11 | 117,947,753 | 117,992,605 | 44,853 |
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