RGS4 regulator of G protein signaling 4
Information
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 2 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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32 |
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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 | |||||||||||
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| 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 | RGP4 |
| SYNONYM | SCZD9 |
| MIM | 602516 OMIM |
| HGNC | HGNC:10000 HGNC |
| Ensembl | ENSG00000117152 Ensembl |
| AllianceGenome | HGNC:10000 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000531057.5 | hg38 | chr1 | 163,069,361 | 163,074,708 | 5,348 |
| ENST00000527809.5 | hg38 | chr1 | 163,069,361 | 163,074,755 | 5,395 |
| ENST00000367906.7 | hg38 | chr1 | 163,072,044 | 163,074,816 | 2,773 |
| ENST00000421743.6 | hg38 | chr1 | 163,068,775 | 163,076,802 | 8,028 |
| ENST00000367908.8 | hg38 | chr1 | 163,069,361 | 163,076,591 | 7,231 |
| ENST00000367909.11 | hg38 | chr1 | 163,069,361 | 163,076,802 | 7,442 |
| ENST00000421743.6 | hg19 | chr1 | 163,038,565 | 163,046,592 | 8,028 |
| ENST00000531057.5 | hg19 | chr1 | 163,039,151 | 163,044,498 | 5,348 |
| ENST00000527809.5 | hg19 | chr1 | 163,039,151 | 163,044,545 | 5,395 |
| ENST00000367908.8 | hg19 | chr1 | 163,039,151 | 163,046,381 | 7,231 |
| ENST00000367909.11 | hg19 | chr1 | 163,039,151 | 163,046,592 | 7,442 |
| ENST00000367906.7 | hg19 | chr1 | 163,041,834 | 163,044,606 | 2,773 |
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