PTCSC3 papillary thyroid carcinoma susceptibility candidate 3
Information
- Symbol
- PTCSC3
- Type
- ncRNA
- Description
- papillary thyroid carcinoma susceptibility candidate 3
- Entrez Gene ID
- 100886964
- Genome
- hg19
- Position
- chr14:36,604,096-36,645,857
- Genome
- hg38
- Position
- chr14:36,134,890-36,176,651
- MIM
- 614821 OMIM
- HGNC
- HGNC:43959 HGNC
- Ensembl
- ENSG00000259104 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 |
Search Word
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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MIM | 614821 OMIM |
HGNC | HGNC:43959 HGNC |
Ensembl | ENSG00000259104 Ensembl |
AllianceGenome | HGNC:43959 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000556013.3 | hg38 | chr14 | 36,134,890 | 36,176,651 | 41,762 |
ENST00000556013.3 | hg19 | chr14 | 36,604,096 | 36,645,857 | 41,762 |
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