"Ambry Genetics"[submitter] AND "MLH1"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 823690	NM_014805.3(EPM2AIP1):c.-134G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 229917	NM_014805.3(EPM2AIP1):c.-137G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 232032	NM_014805.3(EPM2AIP1):c.-139G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1729706	NM_014805.3(EPM2AIP1):c.-144G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 823360	NM_014805.3(EPM2AIP1):c.-145G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 823333	NM_014805.3(EPM2AIP1):c.-146A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1729383	NM_014805.3(EPM2AIP1):c.-147T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1728920	NM_014805.3(EPM2AIP1):c.-151C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1727445	NM_014805.3(EPM2AIP1):c.-163C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1727361	NM_014805.3(EPM2AIP1):c.-164A>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1799257	NM_014805.3(EPM2AIP1):c.-167A>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822588	NM_014805.3(EPM2AIP1):c.-190_-170del21	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141917	NM_014805.3(EPM2AIP1):c.-168G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1799009	NM_014805.3(EPM2AIP1):c.-169G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822658	NM_014805.3(EPM2AIP1):c.-169G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798893	NM_014805.3(EPM2AIP1):c.-170G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822569	NM_014805.3(EPM2AIP1):c.-171G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822494	NM_014805.3(EPM2AIP1):c.-172C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798492	NM_014805.3(EPM2AIP1):c.-173T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798159	NM_014805.3(EPM2AIP1):c.-176A>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1798022	NM_014805.3(EPM2AIP1):c.-177G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 822334	NM_014805.3(EPM2AIP1):c.-178G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1797155	NM_014805.3(EPM2AIP1):c.-184delT	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141675	NM_014805.3(EPM2AIP1):c.-183T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821874	NM_014805.3(EPM2AIP1):c.-185G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821912	NM_014805.3(EPM2AIP1):c.-186C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821909	NM_014805.3(EPM2AIP1):c.-186C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 232066	NM_014805.3(EPM2AIP1):c.-186C>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821831	NM_014805.3(EPM2AIP1):c.-203_-191delCGCTCTTCCTATT	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 229797	NM_014805.3(EPM2AIP1):c.-191T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141996	NM_014805.3(EPM2AIP1):c.-192T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821755	NM_014805.3(EPM2AIP1):c.-197T>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821746	NM_014805.3(EPM2AIP1):c.-198T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1795061	NM_014805.3(EPM2AIP1):c.-201C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1794883	NM_014805.3(EPM2AIP1):c.-202G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 89588	NM_014805.3(EPM2AIP1):c.-202G>C	EPM2AIP1, MLH1	Single nucleotide variant	Lynch syndrome	GLikely benign
Select item 1794532	NM_014805.3(EPM2AIP1):c.-205T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1794426	NM_014805.3(EPM2AIP1):c.-206G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821604	NM_014805.3(EPM2AIP1):c.-208delC	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1794032	NM_014805.3(EPM2AIP1):c.-209G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821564	NM_014805.3(EPM2AIP1):c.-209G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821581	NM_014805.3(EPM2AIP1):c.-210C>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 142740	NM_014805.3(EPM2AIP1):c.-210C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821477	NM_014805.3(EPM2AIP1):c.-216_-215AG[3]	MLH1	Microsatellite	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821549	NM_014805.3(EPM2AIP1):c.-212A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1793479	NM_014805.3(EPM2AIP1):c.-213G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1793365	NM_014805.3(EPM2AIP1):c.-214A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821517	NM_014805.3(EPM2AIP1):c.-214A>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1793215	NM_014805.3(EPM2AIP1):c.-215G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821501	NM_014805.3(EPM2AIP1):c.-215delG	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1792926	NM_014805.3(EPM2AIP1):c.-217T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821415	NM_014805.3(EPM2AIP1):c.-218T>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821435	NM_014805.3(EPM2AIP1):c.-219G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141497	NM_014805.3(EPM2AIP1):c.-219G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 141417	NM_014805.3(EPM2AIP1):c.-220C>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 1792366	NM_014805.3(EPM2AIP1):c.-221G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821390	NM_014805.3(EPM2AIP1):c.-222C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 186425	NM_014805.3(EPM2AIP1):c.-223G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 185671	NM_014805.3(EPM2AIP1):c.-227G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1791313	NM_000249.3(MLH1):c.-243G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1790990	NM_000249.3(MLH1):c.-241A>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821254	NM_000249.3(MLH1):c.-241A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1790148	NM_000249.3(MLH1):c.-235T>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821152	NM_000249.3(MLH1):c.-235T>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821120	NM_000249.3(MLH1):c.-233C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821119	NM_000249.3(MLH1):c.-233C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 142669	NM_000249.3(MLH1):c.-230G>C	MLH1	Single nucleotide variant	Hereditary nonpolyposis colorectal neoplasms +1 more	GLikely benign
Select item 1789235	NM_000249.3(MLH1):c.-229G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 821014	NM_000249.3(MLH1):c.-227A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820965	NM_000249.3(MLH1):c.-224G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820943	NM_000249.3(MLH1):c.-223G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GLikely benign
Select item 820942	NM_000249.3(MLH1):c.-223G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820906	NM_000249.3(MLH1):c.-222G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 185544	NM_000249.3(MLH1):c.-221C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 141665	NM_000249.3(MLH1):c.-221C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820896	NM_000249.3(MLH1):c.-220A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820895	NM_000249.3(MLH1):c.-220A>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1787564	NM_000249.3(MLH1):c.-219G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820882	NM_000249.3(MLH1):c.-219G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 231906	NM_000249.3(MLH1):c.-218T>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820824	NM_000249.3(MLH1):c.-217A>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1787065	NM_000249.3(MLH1):c.-216G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1786871	NM_000249.3(MLH1):c.-215C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1786572	NM_000249.3(MLH1):c.-214_-189del26	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820800	NM_000249.3(MLH1):c.-214delC	MLH1	Deletion	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820735	NM_000249.3(MLH1):c.-215C>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1786713	NM_000249.3(MLH1):c.-214C>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820793	NM_000249.3(MLH1):c.-213G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820792	NM_000249.3(MLH1):c.-213G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820728	NM_000249.3(MLH1):c.-210T>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 231851	NM_000249.3(MLH1):c.-210T>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1785861	NM_000249.3(MLH1):c.-209C>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1785698	NM_000249.3(MLH1):c.-208A>G	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820671	NM_000249.3(MLH1):c.-207G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820669	NM_000249.3(MLH1):c.-207G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1785359	NM_000249.3(MLH1):c.-206G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 232963	NM_000249.3(MLH1):c.-205G>C	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 186388	NM_000249.3(MLH1):c.-205G>T	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 1784881	NM_000249.3(MLH1):c.-203G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 820557	NM_000249.3(MLH1):c.-202G>A	MLH1	Single nucleotide variant	Hereditary cancer-predisposing syndrome	GUncertain significance

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