TFPI2 tissue factor pathway inhibitor 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 8 | 6 |
Likely benign | 0 | 2 |
Uncertain significance | 0 | 20 |
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
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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 |
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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 |
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Target data | : |
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 | PP5 |
SYNONYM | REF1 |
SYNONYM | TFPI-2 |
MIM | 600033 OMIM |
HGNC | HGNC:11761 HGNC |
Ensembl | ENSG00000105825 Ensembl |
AllianceGenome | HGNC:11761 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000650573.1 | hg38 | chr7 | 93,886,471 | 93,890,747 | 4,277 |
ENST00000222543.11 | hg38 | chr7 | 93,885,396 | 93,890,753 | 5,358 |
ENST00000222543.11 | hg19 | chr7 | 93,514,708 | 93,520,065 | 5,358 |
ENST00000650573.1 | hg19 | chr7 | 93,515,783 | 93,520,059 | 4,277 |
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