SAPCD1 suppressor APC domain containing 1
Information
- Symbol
- SAPCD1
- Type
- protein-coding
- Description
- suppressor APC domain containing 1
- Entrez Gene ID
- 401251
- Genome
- hg19
- Position
- chr6:31,730,433-31,732,627
- Genome
- hg38
- Position
- chr6:31,762,656-31,764,850
- HGNC
- HGNC:13938 HGNC
- Ensembl
- ENSG00000228727 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 2 |
Likely benign | 0 | 10 |
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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24 |
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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 |
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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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C6orf26 |
SYNONYM | NG23 |
HGNC | HGNC:13938 HGNC |
Ensembl | ENSG00000228727 Ensembl |
AllianceGenome | HGNC:13938 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000425424.4 | hg38 | chr6 | 31,763,049 | 31,764,828 | 1,780 |
ENST00000415669.4 | hg38 | chr6 | 31,762,656 | 31,764,850 | 2,195 |
ENST00000415669.4 | hg19 | chr6 | 31,730,433 | 31,732,627 | 2,195 |
ENST00000425424.4 | hg19 | chr6 | 31,730,826 | 31,732,605 | 1,780 |
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