List of variants reported as benign for endometrial carcinoma

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Total variants: 27

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.780C>G (p.Ser260=)	rs1805319	0.82058
NM_000251.3(MSH2):c.1661+12G>A	rs3732183	0.40290
NM_000535.7(PMS2):c.1408C>T (p.Pro470Ser)	rs1805321	0.37107
NM_000179.3(MSH6):c.3438+14A>T	rs2020911	0.32279
NM_000535.7(PMS2):c.2570G>C (p.Gly857Ala)	rs1802683	0.30966
NM_000179.3(MSH6):c.540T>C (p.Asp180=)	rs1800935	0.23857
NM_000535.7(PMS2):c.2007-4G>A	rs1805326	0.12350
NM_000535.7(PMS2):c.2007-7C>T	rs55954143	0.12135
NM_000535.7(PMS2):c.2466T>C (p.Leu822=)	rs10000	0.11447
NM_000179.3(MSH6):c.642C>T (p.Tyr214=)	rs1800937	0.07457
NM_000535.7(PMS2):c.59G>A (p.Arg20Gln)	rs10254120	0.07445
NM_000535.7(PMS2):c.1454C>A (p.Thr485Lys)	rs1805323	0.05742
NM_000535.7(PMS2):c.2006+6G>A	rs111905775	0.04390
NM_000535.7(PMS2):c.1531A>G (p.Thr511Ala)	rs2228007	0.02174
NM_000535.7(PMS2):c.1866G>A (p.Met622Ile)	rs1805324	0.01651
NM_004360.5(CDH1):c.1849G>A (p.Ala617Thr)	rs33935154	0.01412
NM_000179.3(MSH6):c.1164C>T (p.His388=)	rs55708305	0.01384
NM_000249.4(MLH1):c.1039-8T>A	rs193922367	0.01153
NM_004360.5(CDH1):c.-71C>G	rs34033771	0.00927
NM_000535.7(PMS2):c.52A>G (p.Ile18Val)	rs63750123	0.00861
NM_000179.3(MSH6):c.2633T>C (p.Val878Ala)	rs2020912	0.00448
NM_006231.4(POLE):c.5334C>T (p.Ala1778=)	rs11146986	0.00205
NM_000535.7(PMS2):c.2340C>T (p.Pro780=)	rs142230276	0.00117
NM_000535.7(PMS2):c.2324A>G (p.Asn775Ser)	rs17420802	0.00025
NM_000535.7(PMS2):c.2253T>C (p.Phe751=)	rs1805325	0.00018
NM_000535.7(PMS2):c.1688G>T (p.Arg563Leu)	rs63750668
NM_000791.4(DHFR):c.-425_-417dup	rs1554066076

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