10[chr] AND 89623000:89730000[chrpos37] - ClinVar - NCBI

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VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 6611981.	NC_000010.11:g.(?_86755016)_(87965482_?)del GRCh37: Chr10:88514773-89725239 GRCh38: Chr10:86755016-87965482	FAM245A, FAM25A, GLUD1, KLLN, LINC00863, LOC111982877, LOC111982878, LOC116216117, LOC121366070, LOC121366071, LOC126860989, LOC126860990, LOC126860991, MINPP1, NUTM2A-AS1, NUTM2D, PAPSS2, MIR4678, MMRN2, LOC124416862, LOC124416863, NUTM2A, ADIRF, ADIRF-AS1, AGAP11, ATAD1, BMPR1A, PTEN, SHLD2, SNCG		Generalized juvenile polyposis/juvenile polyposis coli	Pathogenic (Mar 6, 2019)	criteria provided, single submitter
Select item 6469722.	NC_000010.11:g.(?_86838866)_(87965482_?)del GRCh37: Chr10:88598623-89725239 GRCh38: Chr10:86838866-87965482	ADIRF-AS1, AGAP11, LOC111982877, LOC111982878, LOC116216117, LOC121366070, LOC121366071, LOC124416862, ATAD1, ADIRF, BMPR1A, FAM245A, FAM25A, GLUD1, KLLN, LINC00863, LOC124416863, LOC126860989, LOC126860990, LOC126860991, MINPP1, MIR4678, MMRN2, NUTM2A, NUTM2A-AS1, NUTM2D, PAPSS2, PTEN, SHLD2, SNCG		Generalized juvenile polyposis/juvenile polyposis coli	Pathogenic (Nov 1, 2018)	criteria provided, single submitter
Select item 6601583.	NC_000010.11:g.(?_86875868)_(87894129_?)del GRCh37: Chr10:88635625-89653886 GRCh38: Chr10:86875868-87894129	MMRN2, NUTM2A, NUTM2A-AS1, NUTM2D, PAPSS2, ADIRF, ADIRF-AS1, AGAP11, ATAD1, BMPR1A, FAM245A, FAM25A, GLUD1, KLLN, LINC00863, LOC111982877, LOC111982878, LOC116216117, LOC121366070, LOC121366071, LOC124416862, LOC124416863, LOC126860989, LOC126860990, LOC126860991, MINPP1, MIR4678, PTEN, SHLD2, SNCG		PTEN hamartoma tumor syndrome	Pathogenic (Sep 17, 2018)	criteria provided, single submitter
Select item 5838894.	NC_000010.10:g.(?_89622918)_(89624325_?)dup GRCh37: Chr10:89622918-89624325 GRCh38: Chr10:87863161-87864568	KLLN, PTEN		PTEN hamartoma tumor syndrome	Uncertain significance (Feb 27, 2018)	criteria provided, single submitter
Select item 5842995.	NC_000010.11:g.(?_87863171)_(87864558_?)del GRCh37: Chr10:89622928-89624315 GRCh38: Chr10:87863171-87864558	KLLN, PTEN		PTEN hamartoma tumor syndrome	Pathogenic (Sep 9, 2021)	criteria provided, single submitter
Select item 17714066.	NM_000314.4(PTEN):c.-1032-222_-366del889 GRCh37: Chr10:89622972-89623860 GRCh38: Chr10:87863215-87864103	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 28, 2021)	criteria provided, single submitter
Select item 4888677.	NM_001126049.2(KLLN):c.-756T>G GRCh37: Chr10:89623000 GRCh38: Chr10:87863243	KLLN, PTEN		not provided	Uncertain significance (Sep 29, 2016)	criteria provided, single submitter
Select item 4888688.	NM_001126049.2(KLLN):c.-758G>A GRCh37: Chr10:89623002 GRCh38: Chr10:87863245	KLLN, PTEN		not provided	Uncertain significance (Oct 17, 2017)	criteria provided, single submitter
Select item 4889359.	NM_001126049.2(KLLN):c.-760del GRCh37: Chr10:89623004 GRCh38: Chr10:87863247	KLLN, PTEN		not provided	Uncertain significance (Apr 4, 2018)	criteria provided, single submitter
Select item 48895410.	NM_001126049.2(KLLN):c.-761C>T GRCh37: Chr10:89623005 GRCh38: Chr10:87863248	KLLN, PTEN		not provided	Uncertain significance (Nov 9, 2016)	criteria provided, single submitter
Select item 48877311.	NM_001126049.2(KLLN):c.-761C>G GRCh37: Chr10:89623005 GRCh38: Chr10:87863248	KLLN, PTEN		not provided	Uncertain significance (May 25, 2020)	criteria provided, multiple submitters, no conflicts
Select item 18699112.	NM_001126049.2(KLLN):c.-766G>A GRCh37: Chr10:89623010 GRCh38: Chr10:87863253	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 30, 2014)	criteria provided, single submitter
Select item 14299913.	NM_001126049.2(KLLN):c.-768A>C GRCh37: Chr10:89623012 GRCh38: Chr10:87863255	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 2, 2014)	criteria provided, single submitter
Select item 48885014.	NM_001126049.2(KLLN):c.-770C>A GRCh37: Chr10:89623014 GRCh38: Chr10:87863257	KLLN, PTEN		not provided	Uncertain significance (Oct 27, 2017)	criteria provided, multiple submitters, no conflicts
Select item 175048315.	NM_001126049.2(KLLN):c.-771G>A GRCh37: Chr10:89623015 GRCh38: Chr10:87863258	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 9, 2017)	criteria provided, single submitter
Select item 18952116.	NM_001126049.2(KLLN):c.-772G>A GRCh37: Chr10:89623016 GRCh38: Chr10:87863259	KLLN, PTEN		not provided	Uncertain significance (Aug 11, 2017)	criteria provided, single submitter
Select item 18946917.	NM_001126049.2(KLLN):c.-774G>A GRCh37: Chr10:89623018 GRCh38: Chr10:87863261	KLLN, PTEN		not provided	Uncertain significance (Apr 21, 2014)	criteria provided, single submitter
Select item 23439618.	NM_001126049.2(KLLN):c.-775C>G GRCh37: Chr10:89623019 GRCh38: Chr10:87863262	KLLN, PTEN		not provided	Uncertain significance (Apr 8, 2020)	criteria provided, multiple submitters, no conflicts
Select item 48871419.	NM_001126049.2(KLLN):c.-776G>C GRCh37: Chr10:89623020 GRCh38: Chr10:87863263	KLLN, PTEN		not provided	Uncertain significance (May 11, 2015)	criteria provided, single submitter
Select item 48871520.	NM_001126049.2(KLLN):c.-777C>T GRCh37: Chr10:89623021 GRCh38: Chr10:87863264	KLLN, PTEN		Macrocephaly-autism syndrome, Cowden syndrome 1, Familial meningioma, Malignant tumor of prostate, Glioma susceptibility 2, not provided	Uncertain significance (Mar 15, 2022)	criteria provided, multiple submitters, no conflicts
Select item 23447321.	NM_001126049.2(KLLN):c.-780C>T GRCh37: Chr10:89623024 GRCh38: Chr10:87863267	KLLN, PTEN		not provided	Uncertain significance (Nov 29, 2017)	criteria provided, single submitter
Select item 18943322.	NM_001126049.2(KLLN):c.-794_-783del GRCh37: Chr10:89623027-89623038 GRCh38: Chr10:87863270-87863281	KLLN, PTEN		PTEN hamartoma tumor syndrome	Likely benign (Mar 5, 2019)	reviewed by expert panel FDA Recognized Database
Select item 174623123.	NM_001126049.2(KLLN):c.-785T>C GRCh37: Chr10:89623029 GRCh38: Chr10:87863272	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 13, 2016)	criteria provided, single submitter
Select item 48890024.	NM_001126049.2(KLLN):c.-790G>A GRCh37: Chr10:89623034 GRCh38: Chr10:87863277	KLLN, PTEN		not provided, Hereditary cancer-predisposing syndrome	Uncertain significance (Nov 30, 2019)	criteria provided, multiple submitters, no conflicts
Select item 14298225.	NM_001126049.2(KLLN):c.-797TGC[1] GRCh37: Chr10:89623036-89623038 GRCh38: Chr10:87863279-87863281	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 26, 2014)	criteria provided, single submitter
Select item 12766326.	NM_001126049.2(KLLN):c.-792C>T GRCh37: Chr10:89623036 GRCh38: Chr10:87863279	KLLN, PTEN		PTEN hamartoma tumor syndrome	Uncertain significance (Mar 23, 2020)	reviewed by expert panel FDA Recognized Database
Select item 119223327.	NM_001126049.2(KLLN):c.-801C>T GRCh37: Chr10:89623045 GRCh38: Chr10:87863288	KLLN, PTEN		not specified	Uncertain significance (Aug 2, 2021)	criteria provided, single submitter
Select item 81850428.	NM_001126049.2(KLLN):c.-817_-801del GRCh37: Chr10:89623045-89623061 GRCh38: Chr10:87863288-87863304	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 8, 2019)	criteria provided, single submitter
Select item 48871629.	NM_001126049.2(KLLN):c.-801C>A GRCh37: Chr10:89623045 GRCh38: Chr10:87863288	KLLN, PTEN		not provided	Uncertain significance (Dec 23, 2017)	criteria provided, multiple submitters, no conflicts
Select item 50374830.	NM_001126049.2(KLLN):c.-804_-803delinsAA GRCh37: Chr10:89623047-89623048 GRCh38: Chr10:87863290-87863291	KLLN, PTEN		not provided	Uncertain significance (Aug 29, 2016)	criteria provided, single submitter
Select item 14265231.	NM_001126049.2(KLLN):c.-803T>A GRCh37: Chr10:89623047 GRCh38: Chr10:87863290	KLLN, PTEN		not specified, Hereditary cancer-predisposing syndrome, not provided	Uncertain significance (Jul 19, 2021)	criteria provided, multiple submitters, no conflicts
Select item 14284432.	NM_001126049.2(KLLN):c.-806A>C GRCh37: Chr10:89623050 GRCh38: Chr10:87863293	KLLN, PTEN		not provided, Familial meningioma, Macrocephaly-autism syndrome, Glioma susceptibility 2, Malignant tumor of prostate, Cowden syndrome 1, Cowden syndrome 1, Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 19, 2021)	criteria provided, multiple submitters, no conflicts
Select item 133750933.	NM_001126049.2(KLLN):c.-808G>T GRCh37: Chr10:89623052 GRCh38: Chr10:87863295	KLLN, PTEN		not specified	Uncertain significance (Jan 7, 2020)	criteria provided, single submitter
Select item 48893934.	NM_001126049.2(KLLN):c.-808G>A GRCh37: Chr10:89623052 GRCh38: Chr10:87863295	KLLN, PTEN		not provided	Uncertain significance (Sep 19, 2016)	criteria provided, single submitter
Select item 48886635.	NM_001126049.2(KLLN):c.-809T>C GRCh37: Chr10:89623053 GRCh38: Chr10:87863296	KLLN, PTEN		not provided	Uncertain significance (Mar 7, 2016)	criteria provided, single submitter
Select item 173994636.	NM_001126049.2(KLLN):c.-810C>A GRCh37: Chr10:89623054 GRCh38: Chr10:87863297	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 27, 2017)	criteria provided, single submitter
Select item 48878637.	NM_001126049.2(KLLN):c.-810C>T GRCh37: Chr10:89623054 GRCh38: Chr10:87863297	KLLN, PTEN		Hereditary cancer-predisposing syndrome, not provided	Uncertain significance (Jan 3, 2017)	criteria provided, multiple submitters, no conflicts
Select item 14117038.	NM_001126049.2(KLLN):c.-810C>G GRCh37: Chr10:89623054 GRCh38: Chr10:87863297	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (May 17, 2018)	criteria provided, single submitter
Select item 14078339.	NM_001126049.2(KLLN):c.-812G>T GRCh37: Chr10:89623056 GRCh38: Chr10:87863299	KLLN, PTEN		PTEN hamartoma tumor syndrome	Uncertain significance (Oct 20, 2020)	reviewed by expert panel FDA Recognized Database
Select item 12766240.	NM_001126049.2(KLLN):c.-812G>A GRCh37: Chr10:89623056 GRCh38: Chr10:87863299	KLLN, PTEN		PTEN hamartoma tumor syndrome	Likely benign (Mar 23, 2020)	reviewed by expert panel FDA Recognized Database
Select item 173880141.	NM_001126049.2(KLLN):c.-814C>T GRCh37: Chr10:89623058 GRCh38: Chr10:87863301	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 18, 2020)	criteria provided, single submitter
Select item 81847442.	NM_001126049.2(KLLN):c.-814C>G GRCh37: Chr10:89623058 GRCh38: Chr10:87863301	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Aug 14, 2018)	criteria provided, single submitter
Select item 82226443.	NM_001126049.2(KLLN):c.-817C>T GRCh37: Chr10:89623061 GRCh38: Chr10:87863304	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 6, 2018)	criteria provided, single submitter
Select item 173697244.	NM_001126049.2(KLLN):c.-821C>T GRCh37: Chr10:89623065 GRCh38: Chr10:87863308	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Nov 8, 2019)	criteria provided, single submitter
Select item 81844445.	NM_001126049.2(KLLN):c.-822_-821delinsTT GRCh37: Chr10:89623065-89623066 GRCh38: Chr10:87863308-87863309	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jan 2, 2019)	criteria provided, single submitter
Select item 173665846.	NM_001126049.2(KLLN):c.-822C>G GRCh37: Chr10:89623066 GRCh38: Chr10:87863309	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 6, 2016)	criteria provided, single submitter
Select item 173498247.	NM_001126049.2(KLLN):c.-828C>A GRCh37: Chr10:89623072 GRCh38: Chr10:87863315	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jan 15, 2020)	criteria provided, single submitter
Select item 18736248.	NM_001126049.2(KLLN):c.-828C>T GRCh37: Chr10:89623072 GRCh38: Chr10:87863315	KLLN, PTEN		Familial meningioma, Glioma susceptibility 2, Macrocephaly-autism syndrome, Cowden syndrome 1, Malignant tumor of prostate, VACTERL with hydrocephalus, PTEN hamartoma tumor syndrome, not provided, Hereditary cancer-predisposing syndrome	Uncertain significance (Aug 12, 2019)	criteria provided, multiple submitters, no conflicts
Select item 48871749.	NM_001126049.2(KLLN):c.-829C>T GRCh37: Chr10:89623073 GRCh38: Chr10:87863316	KLLN, PTEN		not provided	Uncertain significance (Feb 17, 2017)	criteria provided, single submitter
Select item 173435950.	NM_001126049.2(KLLN):c.-830G>C GRCh37: Chr10:89623074 GRCh38: Chr10:87863317	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 13, 2017)	criteria provided, single submitter
Select item 81843051.	NM_001126049.2(KLLN):c.-830G>A GRCh37: Chr10:89623074 GRCh38: Chr10:87863317	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 10, 2019)	criteria provided, single submitter
Select item 81842752.	NM_001126049.2(KLLN):c.-831G>C GRCh37: Chr10:89623075 GRCh38: Chr10:87863318	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 18, 2018)	criteria provided, single submitter
Select item 81842653.	NM_001126049.2(KLLN):c.-831G>T GRCh37: Chr10:89623075 GRCh38: Chr10:87863318	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 30, 2019)	criteria provided, single submitter
Select item 82224854.	NM_001126049.2(KLLN):c.-837T>C GRCh37: Chr10:89623081 GRCh38: Chr10:87863324	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Feb 20, 2019)	criteria provided, single submitter
Select item 18700055.	NM_001126049.2(KLLN):c.-837T>G GRCh37: Chr10:89623081 GRCh38: Chr10:87863324	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Feb 14, 2019)	criteria provided, single submitter
Select item 23490056.	NM_001126049.2(KLLN):c.-838T>G GRCh37: Chr10:89623082 GRCh38: Chr10:87863325	KLLN, PTEN		not provided	Uncertain significance (Nov 11, 2016)	criteria provided, single submitter
Select item 48874857.	NM_001126049.2(KLLN):c.-839C>T GRCh37: Chr10:89623083 GRCh38: Chr10:87863326	KLLN, PTEN		not provided	Uncertain significance (Mar 10, 2016)	criteria provided, single submitter
Select item 23486758.	NM_001126049.2(KLLN):c.-840G>T GRCh37: Chr10:89623084 GRCh38: Chr10:87863327	KLLN, PTEN		not provided, Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 20, 2018)	criteria provided, multiple submitters, no conflicts
Select item 23463259.	NM_001126049.2(KLLN):c.-841_-840del GRCh37: Chr10:89623084-89623085 GRCh38: Chr10:87863327-87863328	KLLN, PTEN		Hereditary cancer-predisposing syndrome, not provided	Uncertain significance (Nov 20, 2015)	criteria provided, multiple submitters, no conflicts
Select item 12766160.	NM_001126049.2(KLLN):c.-840G>A GRCh37: Chr10:89623084 GRCh38: Chr10:87863327	KLLN, PTEN		PTEN hamartoma tumor syndrome	Likely benign (Apr 6, 2018)	reviewed by expert panel FDA Recognized Database
Select item 82224061.	NM_001126049.2(KLLN):c.-841G>A GRCh37: Chr10:89623085 GRCh38: Chr10:87863328	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 2, 2018)	criteria provided, single submitter
Select item 48875562.	NM_001126049.2(KLLN):c.-844T>A GRCh37: Chr10:89623088 GRCh38: Chr10:87863331	KLLN, PTEN		not provided	Uncertain significance (Apr 10, 2015)	criteria provided, single submitter
Select item 173012663.	NM_001126049.2(KLLN):c.-845C>G GRCh37: Chr10:89623089 GRCh38: Chr10:87863332	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 23, 2017)	criteria provided, single submitter
Select item 14186464.	NM_001126049.2(KLLN):c.-845C>T GRCh37: Chr10:89623089 GRCh38: Chr10:87863332	KLLN, PTEN		Hereditary cancer-predisposing syndrome, not provided, Familial meningioma, Macrocephaly-autism syndrome, Glioma susceptibility 2, Malignant tumor of prostate, Cowden syndrome 1	Uncertain significance (Feb 14, 2022)	criteria provided, multiple submitters, no conflicts
Select item 48893865.	NM_001126049.2(KLLN):c.-846C>T GRCh37: Chr10:89623090 GRCh38: Chr10:87863333	KLLN, PTEN		not provided	Uncertain significance (Dec 2, 2019)	criteria provided, multiple submitters, no conflicts
Select item 18943466.	NM_001126049.2(KLLN):c.-848_-847insA GRCh37: Chr10:89623091-89623092 GRCh38: Chr10:87863334-87863335	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Aug 6, 2014)	criteria provided, single submitter
Select item 14289267.	NM_001126049.2(KLLN):c.-849C>T GRCh37: Chr10:89623093 GRCh38: Chr10:87863336	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Mar 26, 2014)	criteria provided, single submitter
Select item 50350968.	NM_001126049.2(KLLN):c.-852T>A GRCh37: Chr10:89623096 GRCh38: Chr10:87863339	KLLN, PTEN		not provided	Uncertain significance (Jun 10, 2015)	criteria provided, single submitter
Select item 179902669.	NM_001126049.2(KLLN):c.-857C>A GRCh37: Chr10:89623101 GRCh38: Chr10:87863344	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (May 15, 2017)	criteria provided, single submitter
Select item 179901170.	NM_001126049.2(KLLN):c.-857C>G GRCh37: Chr10:89623101 GRCh38: Chr10:87863344	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jan 3, 2020)	criteria provided, single submitter
Select item 179900271.	NM_001126049.2(KLLN):c.-857C>T GRCh37: Chr10:89623101 GRCh38: Chr10:87863344	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 11, 2020)	criteria provided, single submitter
Select item 179868072.	NM_001126049.2(KLLN):c.-857del GRCh37: Chr10:89623101 GRCh38: Chr10:87863344	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jan 2, 2015)	criteria provided, single submitter
Select item 179872073.	NM_001126049.2(KLLN):c.-858C>T GRCh37: Chr10:89623102 GRCh38: Chr10:87863345	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Oct 20, 2015)	criteria provided, single submitter
Select item 48892274.	NM_001126049.2(KLLN):c.-860G>A GRCh37: Chr10:89623104 GRCh38: Chr10:87863347	KLLN, PTEN		not provided	Uncertain significance (Jun 30, 2016)	criteria provided, single submitter
Select item 23468675.	NM_001126049.2(KLLN):c.-861T>A GRCh37: Chr10:89623105 GRCh38: Chr10:87863348	KLLN, PTEN		not provided	Uncertain significance (Dec 11, 2015)	criteria provided, single submitter
Select item 50350576.	NM_001126049.2(KLLN):c.-862A>G GRCh37: Chr10:89623106 GRCh38: Chr10:87863349	KLLN, PTEN		not provided	Uncertain significance (Dec 23, 2019)	criteria provided, multiple submitters, no conflicts
Select item 50351177.	NM_001126049.2(KLLN):c.-870T>C GRCh37: Chr10:89623114 GRCh38: Chr10:87863357	KLLN, PTEN		not provided	Uncertain significance (Jul 30, 2018)	criteria provided, multiple submitters, no conflicts
Select item 48893078.	NM_001126049.2(KLLN):c.-873C>A GRCh37: Chr10:89623117 GRCh38: Chr10:87863360	KLLN, PTEN		not provided	Uncertain significance (Aug 8, 2016)	criteria provided, single submitter
Select item 82219179.	NM_001126049.2(KLLN):c.-874G>A GRCh37: Chr10:89623118 GRCh38: Chr10:87863361	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jun 4, 2019)	criteria provided, single submitter
Select item 81836680.	NM_001126049.2(KLLN):c.-879C>T GRCh37: Chr10:89623123 GRCh38: Chr10:87863366	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 5, 2018)	criteria provided, single submitter
Select item 99323481.	NM_001126049.2(KLLN):c.-881G>A GRCh37: Chr10:89623125 GRCh38: Chr10:87863368	KLLN, PTEN		not provided	Uncertain significance (Jan 20, 2020)	criteria provided, single submitter
Select item 48888582.	NM_001126049.2(KLLN):c.-882A>C GRCh37: Chr10:89623126 GRCh38: Chr10:87863369	KLLN, PTEN		not provided	Uncertain significance (Aug 31, 2017)	criteria provided, single submitter
Select item 48879183.	NM_001126049.2(KLLN):c.-882A>G GRCh37: Chr10:89623126 GRCh38: Chr10:87863369	KLLN, PTEN		not provided	Uncertain significance (Oct 14, 2015)	criteria provided, single submitter
Select item 41843084.	NM_001126049.2(KLLN):c.-884C>T GRCh37: Chr10:89623128 GRCh38: Chr10:87863371	KLLN, PTEN		Hereditary cancer-predisposing syndrome, not specified	Uncertain significance (Jul 14, 2017)	criteria provided, multiple submitters, no conflicts
Select item 82216085.	NM_001126049.2(KLLN):c.-885C>T GRCh37: Chr10:89623129 GRCh38: Chr10:87863372	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 2, 2018)	criteria provided, single submitter
Select item 82215886.	NM_001126049.2(KLLN):c.-886C>A GRCh37: Chr10:89623130 GRCh38: Chr10:87863373	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Apr 8, 2019)	criteria provided, single submitter
Select item 18947087.	NM_001126049.2(KLLN):c.-886C>T GRCh37: Chr10:89623130 GRCh38: Chr10:87863373	KLLN, PTEN		not provided	Uncertain significance (Aug 20, 2014)	criteria provided, single submitter
Select item 54881688.	NM_001126049.2(KLLN):c.-887C>T GRCh37: Chr10:89623131 GRCh38: Chr10:87863374	KLLN, PTEN		Cowden syndrome 1	Uncertain significance (Dec 9, 2017)	criteria provided, single submitter
Select item 18947189.	NM_001126049.2(KLLN):c.-887C>A GRCh37: Chr10:89623131 GRCh38: Chr10:87863374	KLLN, PTEN		not provided	Uncertain significance (Oct 10, 2016)	criteria provided, single submitter
Select item 18943590.	NM_001126049.2(KLLN):c.-914_-889del GRCh37: Chr10:89623133-89623158 GRCh38: Chr10:87863376-87863401	KLLN, PTEN		not provided, Hereditary cancer-predisposing syndrome	Conflicting interpretations of pathogenicity (Aug 19, 2021)	criteria provided, conflicting interpretations
Select item 22494291.	NM_001126049.2(KLLN):c.-897A>G GRCh37: Chr10:89623141 GRCh38: Chr10:87863384	KLLN, PTEN		PTEN hamartoma tumor syndrome	Benign (Nov 5, 2015)	criteria provided, single submitter
Select item 48878892.	NM_001126049.2(KLLN):c.-898G>C GRCh37: Chr10:89623142 GRCh38: Chr10:87863385	KLLN, PTEN		not provided	Uncertain significance (Feb 10, 2021)	criteria provided, single submitter
Select item 12766093.	NM_001126049.2(KLLN):c.-898G>A GRCh37: Chr10:89623142 GRCh38: Chr10:87863385	KLLN, PTEN		PTEN hamartoma tumor syndrome	Likely benign (Nov 28, 2018)	reviewed by expert panel FDA Recognized Database
Select item 48892194.	NM_001126049.2(KLLN):c.-899C>A GRCh37: Chr10:89623143 GRCh38: Chr10:87863386	KLLN, PTEN		not provided	Uncertain significance (Nov 19, 2018)	criteria provided, single submitter
Select item 14205895.	NM_001126049.2(KLLN):c.-899C>G GRCh37: Chr10:89623143 GRCh38: Chr10:87863386	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 13, 2013)	criteria provided, single submitter
Select item 81833796.	NM_001126049.2(KLLN):c.-902G>C GRCh37: Chr10:89623146 GRCh38: Chr10:87863389	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Sep 6, 2018)	criteria provided, single submitter
Select item 14160497.	NM_001126049.2(KLLN):c.-902G>A GRCh37: Chr10:89623146 GRCh38: Chr10:87863389	KLLN, PTEN		not provided, Hereditary cancer-predisposing syndrome	Uncertain significance (Dec 13, 2017)	criteria provided, multiple submitters, no conflicts
Select item 18554198.	NM_001126049.2(KLLN):c.-903G>A GRCh37: Chr10:89623147 GRCh38: Chr10:87863390	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Jul 11, 2014)	criteria provided, single submitter
Select item 14209799.	NM_001126049.2(KLLN):c.-903G>C GRCh37: Chr10:89623147 GRCh38: Chr10:87863390	KLLN, PTEN		Hereditary cancer-predisposing syndrome	Uncertain significance (Sep 4, 2019)	criteria provided, single submitter
Select item 141878100.	NM_001126049.2(KLLN):c.-906C>G GRCh37: Chr10:89623150 GRCh38: Chr10:87863393	KLLN, PTEN		not provided, Hereditary cancer-predisposing syndrome	Uncertain significance (Feb 16, 2018)	criteria provided, multiple submitters, no conflicts

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