Developers can now request access to the COGVIC API by sending an email to info@mendel-genes.com, which should include the following:

• Basic developer information: name or company name, contact name, mobile phone number, email address
• Data required for application: list the mutation site information or interpretation information required for application, and briefly describe the role of these information in application

After completing your application, you will get a client_id with a duration of 15 days:

• client_id Secret key

The document directory

• Obtain Authorization
• API Input Parameters
• Get Gene Informations

Obtain Authorization

Send http://www.cogvic.vip/COGVIC/getToken?client_id=client_id to the server in your application with the following parameters:

• client_id What we offer you

Then you will get a token with a duration of 2 hours.

If successful, you will receive a JSON response like this:

{"msg":"success","token":"bd990fbb"}

Otherwise, you will receive an error response：

{"msg":"client_id Not Found","code":"404"}

API Input Parameters

Parameter	Type	Default Value	Reference Data	Explain
pageNum	Integer	1		Page Number
pageSize	Interger	5		Number of Pages
searchKey	String		gene,rsid,chromosome,population	Key Column
searchValue	String			Key Column Value
sort	String		id,dbsnpId	The key
order	String		asc,desc	The order
token	String			Token

Get Gene Informations

Send to the server using the following format:

http://www.cogvic.vip/COGVIC/getGeneMsg?searchKey=searchKey&searchValue=searchValue&sort=sort&order=order&token=token

If successful, you will receive a JSON response like this:

                            {
                                "msg": "success",
                                "total": 3,
                                "mutaSum": 0,
                                "rows": [
                                    {
                                        "chromosome": "11",
                                        "clinvarId": "-",
                                        "dbsnpId": ".",
                                        "disease": ".",
                                        "gene": "DDB2",
                                        "id": 221,
                                        "molecularConsequence": "-",
                                        "mutationineastasia": "0",
                                        "nucleotideChange": "DDB2:NM_000107:exon2:c.C259T:p.Q87X,DDB2:NM_001300734:exon2:c.C259T:p.Q87X",
                                        "nucleotidesAlt": "T",
                                        "nucleotidesRef": "C",
                                        "position": "47238018",
                                        "variantType": "stopgain"
                                    },
                                    {
                                        "chromosome": "11",
                                        "clinvarId": "-",
                                        "dbsnpId": "rs144989465",
                                        "disease": ".",
                                        "gene": "DDB2",
                                        "id": 222,
                                        "molecularConsequence": "-",
                                        "mutationineastasia": "0",
                                        "nucleotideChange": "DDB2:NM_000107:exon5:c.C640T:p.R214X",
                                        "nucleotidesAlt": "T",
                                        "nucleotidesRef": "C",
                                        "position": "47256161",
                                        "variantType": "stopgain"
                                    },
                                    {
                                        "chromosome": "11",
                                        "clinvarId": "8788",
                                        "dbsnpId": "rs121434640",
                                        "disease": "Xeroderma_pigmentosum,_group_E",
                                        "gene": "DDB2",
                                        "id": 223,
                                        "molecularConsequence": "SO:0001583|missense_variant,SO:0001627|intron_variant",
                                        "mutationineastasia": "0",
                                        "nucleotideChange": "DDB2:NM_000107:exon6:c.G818A:p.R273H",
                                        "nucleotidesAlt": "A",
                                        "nucleotidesRef": "G",
                                        "position": "47256423",
                                        "variantType": "nonsynonymous SNV"
                                    }
                                ],
                                "type": "gene"
                            }
                        

Otherwise, you will receive an error response：

{"msg":"Token Not Found","code":"404"}

{"msg":"The parameter cannot be empty","code":"405"}