SAMD10 sterile alpha motif domain containing 10
Information
- Symbol
- SAMD10
- Type
- protein-coding
- Description
- sterile alpha motif domain containing 10
- Entrez Gene ID
- 140700
- Genome
- hg19
- Position
- chr20:62,605,469-62,610,995
- Genome
- hg38
- Position
- chr20:63,974,116-63,979,642
- HGNC
- HGNC:16129 HGNC
- Ensembl
- ENSG00000130590 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 32 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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34 |
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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 | : |
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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 |
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SYNONYM | C20orf136 |
SYNONYM | dJ591C20 |
SYNONYM | dJ591C20.7 |
HGNC | HGNC:16129 HGNC |
Ensembl | ENSG00000130590 Ensembl |
AllianceGenome | HGNC:16129 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000369886.8 | hg38 | chr20 | 63,974,116 | 63,979,642 | 5,527 |
ENST00000369886.8 | hg19 | chr20 | 62,605,469 | 62,610,995 | 5,527 |
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