PROC protein C, inactivator of coagulation factors Va and VIIIa
Information
- Symbol
- PROC
- Type
- protein-coding
- Description
- protein C, inactivator of coagulation factors Va and VIIIa
- Entrez Gene ID
- 5624
- Genome
- hg19
- Position
- chr2:128,177,458-128,186,559
- Genome
- hg38
- Position
- chr2:127,419,882-127,428,983
- MIM
- 612283 OMIM
- HGNC
- HGNC:9451 HGNC
- Ensembl
- ENSG00000115718 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 10 | 100 |
Likely pathogenic | 0 | 114 |
Benign | 0 | 54 |
Likely benign | 0 | 172 |
Conflicting classifications of pathogenicity | 0 | 56 |
not provided | 0 | 2 |
Uncertain significance | 0 | 272 |
Ranking
ClinVar | |
---|---|
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0 |
![]() |
0 |
![]() |
142 |
![]() |
488 |
![]() |
28 |
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
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | APC |
SYNONYM | PC |
SYNONYM | PROC1 |
SYNONYM | THPH3 |
SYNONYM | THPH4 |
MIM | 612283 OMIM |
HGNC | HGNC:9451 HGNC |
Ensembl | ENSG00000115718 Ensembl |
AllianceGenome | HGNC:9451 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000409048.1 | hg38 | chr2 | 127,419,882 | 127,428,983 | 9,102 |
ENST00000234071.8 | hg38 | chr2 | 127,418,427 | 127,429,242 | 10,816 |
ENST00000234071.8 | hg19 | chr2 | 128,176,003 | 128,186,818 | 10,816 |
ENST00000409048.1 | hg19 | chr2 | 128,177,458 | 128,186,559 | 9,102 |
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