diff --git a/app/common.py b/app/common.py
index f64261ba..f671b452 100644
--- a/app/common.py
+++ b/app/common.py
@@ -743,7 +743,6 @@ def create_molecular_consequence_profile(molecular_consequence, subject, vids):
     return resource
 
 
-
 def create_tx_implication_profile_civic(implication, subject, vids):
     resource = OrderedDict()
     resource["resourceType"] = "Observation"
@@ -1874,6 +1873,7 @@ def query_transcript(transcript):
 
     return results
 
+
 def query_molecular_consequences_by_variants(normalized_variant_list, feature_consequence_list, query):
     variant_list = []
     for item in normalized_variant_list:
diff --git a/app/endpoints.py b/app/endpoints.py
index 6318ddf5..98cee752 100644
--- a/app/endpoints.py
+++ b/app/endpoints.py
@@ -1159,6 +1159,7 @@ def find_subject_dx_implications(
 
         return jsonify(result)
 
+
 def find_subject_molecular_consequences(
         subject, variants=None, ranges=None, featureConsequence=None, testIdentifiers=None, testDateRange=None,
         specimenIdentifiers=None, genomicSourceClass=None):
diff --git a/utilities/mongo_utilities.py b/utilities/mongo_utilities.py
deleted file mode 100644
index 96db7efa..00000000
--- a/utilities/mongo_utilities.py
+++ /dev/null
@@ -1,46 +0,0 @@
-import pymongo
-
-# can use this script to help debug mongo queries
-
-# MongoDB Client URIs
-FHIR_genomics_data_client_uri = "mongodb+srv://download:download@cluster0.8ianr.mongodb.net/FHIRGenomicsData"
-utilities_data_client_uri = "mongodb+srv://download:download@cluster0.8ianr.mongodb.net/UtilitiesData"
-
-# MongoDB Clients
-client = pymongo.MongoClient(FHIR_genomics_data_client_uri)
-utilities_client = pymongo.MongoClient(utilities_data_client_uri)
-
-# Databases
-db = client.FHIRGenomicsData
-utilities_db = utilities_client.UtilitiesData
-
-
-# Collections
-variants = db.Variants
-molconseqs = db.MolecConseq
-tests = db.Tests
-
-
-# Create records
-
-
-# READ records
-# print(variants.find_one({"patientID":{"$in":["HG00403"]}}))
-
-# print(molconseqs.find_one({"patientID":"TCGA-DD-A1EH","variantID":{"$in": ["0a4f15c4b50b4d3799f223735029bf9c"]}}))
-
-# results=(molconseqs.aggregate([{"$match":{"patientID": "TCGA-DD-A1EH","variantID":{"$in":["0a4f15c4b50b4d3799f223735029bf9c"]}}}]))
-# for result in results:
-#     print(result)
-
-matchPortion = {'$match':{'patientID':'TCGA-DD-A1EH','SPDI':{'$in':['NC_000001.10:27105549:C:T','NC_000001.10:27106893::T','NC_000007.13:41729606:G:A']}}}
-lookupPortion = {'$lookup':{'from':'MolecConseq','let':{'myvariant_id':'$_id'},'pipeline':[{'$match':{'$expr':{'$and':[{'$or':[{'$eq':['$variantID','$$myvariant_id']}]}]}}}],'as':'molecularConsequenceMatches'}}
-addFieldsPortion = {'$addFields':{}}
-secondMatchPortion = {'$match':{'molecularConsequenceMatches':{'$exists':True,'$not':{'$size':0}}}}
-query = [matchPortion,lookupPortion,addFieldsPortion,secondMatchPortion]
-print(query)
-results=(variants.aggregate(query))
-for result in results:
-    print(result)
-
-