PTH parathyroid hormone
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 6 |
Likely pathogenic | 0 | 8 |
Benign | 4 | 20 |
Likely benign | 0 | 12 |
Uncertain significance | 0 | 26 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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12 |
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50 |
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10 |
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
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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 |
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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 | FIH1 |
SYNONYM | PTH1 |
MIM | 168450 OMIM |
HGNC | HGNC:9606 HGNC |
Ensembl | ENSG00000152266 Ensembl |
AllianceGenome | HGNC:9606 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000282091.6 | hg38 | chr11 | 13,492,054 | 13,495,997 | 3,944 |
ENST00000529816.1 | hg38 | chr11 | 13,492,099 | 13,496,181 | 4,083 |
ENST00000282091.6 | hg19 | chr11 | 13,513,601 | 13,517,544 | 3,944 |
ENST00000529816.1 | hg19 | chr11 | 13,513,646 | 13,517,728 | 4,083 |
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