ARMC6 armadillo repeat containing 6
Information
- Symbol
- ARMC6
- Type
- protein-coding
- Description
- armadillo repeat containing 6
- Entrez Gene ID
- 93436
- Genome
- hg19
- Position
- chr19:19,144,412-19,168,985
- Genome
- hg38
- Position
- chr19:19,033,603-19,058,176
- HGNC
- HGNC:25049 HGNC
- Ensembl
- ENSG00000105676 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 62 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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64 |
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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 | : |
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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| Filtering | : |
| 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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| Filtering | : |
| 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 | R30923_1 |
| HGNC | HGNC:25049 HGNC |
| Ensembl | ENSG00000105676 Ensembl |
| AllianceGenome | HGNC:25049 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000546344.5 | hg38 | chr19 | 19,033,613 | 19,059,501 | 25,889 |
| ENST00000392336.7 | hg38 | chr19 | 19,034,103 | 19,057,881 | 23,779 |
| ENST00000392335.6 | hg38 | chr19 | 19,033,575 | 19,058,178 | 24,604 |
| ENST00000535612.6 | hg38 | chr19 | 19,033,603 | 19,058,176 | 24,574 |
| ENST00000269932.10 | hg38 | chr19 | 19,033,610 | 19,058,159 | 24,550 |
| ENST00000392335.6 | hg19 | chr19 | 19,144,384 | 19,168,987 | 24,604 |
| ENST00000535612.6 | hg19 | chr19 | 19,144,412 | 19,168,985 | 24,574 |
| ENST00000269932.10 | hg19 | chr19 | 19,144,419 | 19,168,968 | 24,550 |
| ENST00000392336.7 | hg19 | chr19 | 19,144,912 | 19,168,690 | 23,779 |
| ENST00000546344.5 | hg19 | chr19 | 19,144,422 | 19,170,310 | 25,889 |
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