NTPCR nucleoside-triphosphatase, cancer-related
Information
- Symbol
- NTPCR
- Type
- protein-coding
- Description
- nucleoside-triphosphatase, cancer-related
- Entrez Gene ID
- 84284
- Genome
- hg19
- Position
- chr1:233,086,357-233,119,628
- Genome
- hg38
- Position
- chr1:232,950,611-232,983,882
- HGNC
- HGNC:28204 HGNC
- Ensembl
- ENSG00000135778 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 40 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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42 |
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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 |
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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 |
---|---|
SYNONYM | C1orf57 |
SYNONYM | HCR-NTPase |
SYNONYM | THEP1 |
HGNC | HGNC:28204 HGNC |
Ensembl | ENSG00000135778 Ensembl |
AllianceGenome | HGNC:28204 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000366628.10 | hg38 | chr1 | 232,950,611 | 232,983,882 | 33,272 |
ENST00000366627.4 | hg38 | chr1 | 232,950,640 | 232,977,528 | 26,889 |
ENST00000366628.10 | hg19 | chr1 | 233,086,357 | 233,119,628 | 33,272 |
ENST00000366627.4 | hg19 | chr1 | 233,086,386 | 233,113,274 | 26,889 |
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