SRRM5 serine/arginine repetitive matrix 5
Information
- Symbol
- SRRM5
- Type
- protein-coding
- Description
- serine/arginine repetitive matrix 5
- Entrez Gene ID
- 100170229
- Genome
- hg19
- Position
- chr19:44,100,769-44,118,649
- Genome
- hg38
- Position
- chr19:43,596,617-43,614,497
- HGNC
- HGNC:37248 HGNC
- Ensembl
- ENSG00000226763 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 18 |
not provided | 1 | 0 |
Uncertain significance | 0 | 110 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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128 |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
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 | ZNF576 |
HGNC | HGNC:37248 HGNC |
Ensembl | ENSG00000226763 Ensembl |
AllianceGenome | HGNC:37248 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000417606.3 | hg38 | chr19 | 43,612,088 | 43,614,498 | 2,411 |
ENST00000607544.1 | hg38 | chr19 | 43,596,617 | 43,614,497 | 17,881 |
ENST00000607544.1 | hg19 | chr19 | 44,100,769 | 44,118,649 | 17,881 |
ENST00000417606.3 | hg19 | chr19 | 44,116,240 | 44,118,650 | 2,411 |
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