MIR29C microRNA 29c
Clinical Significance
| MGeND | ClinVar | |
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| not provided | 1 | 0 |
Ranking
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Frequency
EXAC_EAS
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HGVD
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TOMMO
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Gene
Position
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Variants
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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 | |||||||||||
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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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MIRN29C |
| SYNONYM | miRNA29C |
| SYNONYM | mir-29c |
| MIM | 610784 OMIM |
| HGNC | HGNC:31621 HGNC |
| Ensembl | ENSG00000284214 Ensembl |
| miRBase | MI0000735 |
| AllianceGenome | HGNC:31621 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000385231.3 | hg38 | chr1 | 207,801,852 | 207,801,939 | 88 |
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