H3C14 H3 clustered histone 14
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 4 | 0 |
Ranking
| ClinVar | |
|---|---|
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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
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | H3 |
| SYNONYM | H3.2 |
| SYNONYM | H3/M |
| SYNONYM | H3C13 |
| SYNONYM | H3C15 |
| SYNONYM | H3F2 |
| SYNONYM | H3FM |
| SYNONYM | H3FN |
| SYNONYM | HIST2H3C |
| MIM | 142780 OMIM |
| HGNC | HGNC:20503 HGNC |
| Ensembl | ENSG00000203811 Ensembl |
| AllianceGenome | HGNC:20503 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000369158.2 | hg38 | chr1 | 149,840,687 | 149,841,208 | 522 |
| ENST00000369158.2 | hg19 | chr1 | 149,812,259 | 149,812,780 | 522 |
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