VCF2 VCP nuclear cofactor family member 2
Information
- Symbol
- VCF2
- Type
- protein-coding
- Description
- VCP nuclear cofactor family member 2
- Entrez Gene ID
- 90736
- Genome
- hg19
- Position
- chrX:55,171,678-55,187,628
- Genome
- hg38
- Position
- chrX:55,145,245-55,161,195
- HGNC
- HGNC:25085 HGNC
- Ensembl
- ENSG00000182518 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
not provided | 6 | 0 |
Uncertain significance | 0 | 12 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
![]() |
4 |
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 | |||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | CXorf44 |
SYNONYM | FAM104B |
HGNC | HGNC:25085 HGNC |
Ensembl | ENSG00000182518 Ensembl |
AllianceGenome | HGNC:25085 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000358460.8 | hg38 | chrX | 55,143,102 | 55,161,310 | 18,209 |
ENST00000425133.2 | hg38 | chrX | 55,145,245 | 55,161,195 | 15,951 |
ENST00000477847.6 | hg38 | chrX | 55,145,387 | 55,161,119 | 15,733 |
ENST00000489298.1 | hg38 | chrX | 55,145,938 | 55,161,102 | 15,165 |
ENST00000685693.1 | hg38 | chrX | 55,143,102 | 55,161,185 | 18,084 |
ENST00000472571.2 | hg38 | chrX | 55,145,356 | 55,161,182 | 15,827 |
ENST00000332132.8 | hg38 | chrX | 55,143,102 | 55,161,195 | 18,094 |
ENST00000685693.1 | hg19 | chrX | 55,169,535 | 55,187,618 | 18,084 |
ENST00000332132.8 | hg19 | chrX | 55,169,535 | 55,187,628 | 18,094 |
ENST00000358460.8 | hg19 | chrX | 55,169,535 | 55,187,743 | 18,209 |
ENST00000425133.2 | hg19 | chrX | 55,171,678 | 55,187,628 | 15,951 |
ENST00000472571.2 | hg19 | chrX | 55,171,789 | 55,187,615 | 15,827 |
ENST00000477847.6 | hg19 | chrX | 55,171,820 | 55,187,552 | 15,733 |
ENST00000489298.1 | hg19 | chrX | 55,172,371 | 55,187,535 | 15,165 |
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