RNASE1 ribonuclease A family member 1, pancreatic
Information
- Symbol
- RNASE1
- Type
- protein-coding
- Description
- ribonuclease A family member 1, pancreatic
- Entrez Gene ID
- 6035
- Genome
- hg19
- Position
- chr14:21,269,387-21,271,003
- Genome
- hg38
- Position
- chr14:20,801,228-20,802,844
- MIM
- 180440 OMIM
- HGNC
- HGNC:10044 HGNC
- Ensembl
- ENSG00000129538 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 16 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | RAC1 |
SYNONYM | RIB1 |
SYNONYM | RNS1 |
MIM | 180440 OMIM |
HGNC | HGNC:10044 HGNC |
Ensembl | ENSG00000129538 Ensembl |
AllianceGenome | HGNC:10044 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000412779.2 | hg38 | chr14 | 20,801,356 | 20,802,406 | 1,051 |
ENST00000555698.5 | hg38 | chr14 | 20,801,394 | 20,802,848 | 1,455 |
ENST00000397970.4 | hg38 | chr14 | 20,801,460 | 20,802,848 | 1,389 |
ENST00000340900.3 | hg38 | chr14 | 20,801,346 | 20,802,855 | 1,510 |
ENST00000397967.5 | hg38 | chr14 | 20,801,228 | 20,802,844 | 1,617 |
ENST00000397967.5 | hg19 | chr14 | 21,269,387 | 21,271,003 | 1,617 |
ENST00000340900.3 | hg19 | chr14 | 21,269,505 | 21,271,014 | 1,510 |
ENST00000412779.2 | hg19 | chr14 | 21,269,515 | 21,270,565 | 1,051 |
ENST00000555698.5 | hg19 | chr14 | 21,269,553 | 21,271,007 | 1,455 |
ENST00000397970.4 | hg19 | chr14 | 21,269,619 | 21,271,007 | 1,389 |
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