PROSER3 proline and serine rich 3
Information
- Symbol
- PROSER3
- Type
- protein-coding
- Description
- proline and serine rich 3
- Entrez Gene ID
- 148137
- Genome
- hg19
- Position
- chr19:36,249,077-36,262,068
- Genome
- hg38
- Position
- chr19:35,758,176-35,771,166
- HGNC
- HGNC:25204 HGNC
- Ensembl
- ENSG00000167595 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
not provided | 1 | 0 |
Uncertain significance | 0 | 38 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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44 |
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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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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 | C19orf55 |
HGNC | HGNC:25204 HGNC |
Ensembl | ENSG00000167595 Ensembl |
AllianceGenome | HGNC:25204 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000537459.5 | hg38 | chr19 | 35,758,194 | 35,762,563 | 4,370 |
ENST00000646935.2 | hg38 | chr19 | 35,758,176 | 35,771,166 | 12,991 |
ENST00000421853.6 | hg38 | chr19 | 35,758,198 | 35,762,745 | 4,548 |
ENST00000696042.1 | hg38 | chr19 | 35,758,153 | 35,769,371 | 11,219 |
ENST00000696041.1 | hg38 | chr19 | 35,758,153 | 35,769,371 | 11,219 |
ENST00000696040.1 | hg38 | chr19 | 35,758,146 | 35,769,371 | 11,226 |
ENST00000536950.5 | hg38 | chr19 | 35,758,179 | 35,763,045 | 4,867 |
ENST00000396908.9 | hg38 | chr19 | 35,758,153 | 35,771,166 | 13,014 |
ENST00000396908.9 | hg19 | chr19 | 36,249,054 | 36,262,068 | 13,015 |
ENST00000536950.5 | hg19 | chr19 | 36,249,080 | 36,253,946 | 4,867 |
ENST00000421853.6 | hg19 | chr19 | 36,249,099 | 36,253,646 | 4,548 |
ENST00000537459.5 | hg19 | chr19 | 36,249,095 | 36,253,464 | 4,370 |
ENST00000646935.2 | hg19 | chr19 | 36,249,077 | 36,262,068 | 12,992 |
ENST00000696040.1 | hg19 | chr19 | 36,249,047 | 36,260,273 | 11,227 |
ENST00000696042.1 | hg19 | chr19 | 36,249,054 | 36,260,273 | 11,220 |
ENST00000696041.1 | hg19 | chr19 | 36,249,054 | 36,260,273 | 11,220 |
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