Assay Details
Target Gene Details
Entrez Gene ID: | 6037 |
Gene Name: | ribonuclease A family member 3 |
Gene Aliases: |
ECP, RAF1, RNS3 |
Location: |
Chr.14:20891403-20892348 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
RNASE3 | NM_002935.2 | NP_002926.2 | ||
BC096060.1 | AAH96060.1 | |||
BC096061.3 | AAH96061.1 | |||
BC096062.3 | AAH96062.1 | |||
BX280390.1 | ||||
M28128.1 | AAA50283.1 | |||
X15161.1 | CAA33251.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv498822 | Chr.14:20881516 - 20945676 on Build GRCh38 | Loss |
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dgv1800n100 | Chr.14:20877548 - 20957189 on Build GRCh38 | Gain |
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esv2759972 | Chr.14:20747949 - 21003455 on Build GRCh38 | Gain+Loss |
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nsv1044554 | Chr.14:20865928 - 20987933 on Build GRCh38 | Gain |
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esv3892467 | Chr.14:20876009 - 20952929 on Build GRCh38 | Gain+Loss |
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nsv470622 | Chr.14:20870665 - 21000992 on Build GRCh38 | Loss |
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nsv832740 | Chr.14:20863901 - 21076893 on Build GRCh38 | Gain |
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nsv436831 | Chr.14:20887999 - 20947016 on Build GRCh38 | Insertion |
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dgv363n67 | Chr.14:20875340 - 20955179 on Build GRCh38 | Gain |
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esv2673725 | Chr.14:20889599 - 20917545 on Build GRCh38 | Deletion |
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nsv9121 | Chr.14:20873744 - 20958490 on Build GRCh38 | Gain+Loss |
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esv29488 | Chr.14:20881501 - 20955354 on Build GRCh38 | Loss |
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nsv983967 | Chr.14:20873752 - 20965496 on Build GRCh38 | Duplication |
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dgv1798n100 | Chr.14:20870300 - 20957189 on Build GRCh38 | Gain+Loss |
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nsv1204 | Chr.14:20875245 - 20949449 on Build GRCh38 | Deletion |
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nsv817619 | Chr.14:20875005 - 20945443 on Build GRCh38 | Gain |
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dgv380e214 | Chr.14:20886539 - 20948460 on Build GRCh38 | Gain |
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nsv433274 | Chr.14:20889996 - 20937726 on Build GRCh38 | Loss |
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nsv1205 | Chr.14:20876553 - 20909051 on Build GRCh38 | Insertion |
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dgv1799n100 | Chr.14:20872480 - 20941810 on Build GRCh38 | Loss |
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dgv1802n100 | Chr.14:20881449 - 20964296 on Build GRCh38 | Loss |
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nsv442680 | Chr.14:20881447 - 20941822 on Build GRCh38 | Gain+Loss |
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dgv1801n100 | Chr.14:20880514 - 20934425 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Additional Information:
For this assay, SNP(s) [rs570114626] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
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Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)