List of variants reported as benign for benign neoplasm by Genome-Nilou Lab

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Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_133171.5(ELMO2):c.1980T>C (p.Asp660=)	rs2257495	0.98384
NM_003000.3(SDHB):c.201-36G>T	rs1022580	0.95416
NM_003000.3(SDHB):c.18C>A (p.Ala6=)	rs2746462	0.95374
NM_153490.3(KRT13):c.892A>G (p.Thr298Ala)	rs4796697	0.91638
NM_153490.3(KRT13):c.114C>T (p.Ser38=)	rs8182306	0.87031
NM_020975.6(RET):c.3187+47T>C	rs2075912	0.84041
NM_153490.3(KRT13):c.735+10A>G	rs7211835	0.83623
NM_015922.3(NSDHL):c.132T>G (p.Gly44=)	rs5969919	0.83345
NM_005401.5(PTPN14):c.-26G>A	rs10864100	0.83031
NM_005401.5(PTPN14):c.2688+26C>T	rs3013451	0.82386
NM_005401.5(PTPN14):c.978A>G (p.Arg326=)	rs7550799	0.82382
NM_005401.5(PTPN14):c.3252A>G (p.Glu1084=)	rs1135352	0.81332
NM_153490.3(KRT13):c.897+6C>T	rs4796698	0.81266
NM_020975.6(RET):c.2307G>T (p.Leu769=)	rs1800861	0.79547
NM_020975.6(RET):c.135A>G (p.Ala45=)	rs1800858	0.79274
NM_020975.6(RET):c.1296A>G (p.Ala432=)	rs1800860	0.74268
NM_153490.3(KRT13):c.560C>T (p.Ala187Val)	rs9891361	0.71565
NM_020975.6(RET):c.867+48A>G	rs2435352	0.37996
NM_005401.5(PTPN14):c.758+5T>G	rs11580603	0.37880
NM_001365951.3(KIF1B):c.1777+10C>T	rs3753037	0.26503
NM_001365951.3(KIF1B):c.720+17C>T	rs1339458	0.25792
NM_001365951.3(KIF1B):c.285C>G (p.Ala95=)	rs12402052	0.24010
NM_001365951.3(KIF1B):c.5301C>A (p.Thr1767=)	rs11121552	0.23676
NM_005401.5(PTPN14):c.*26G>A	rs2291831	0.15689
NM_003002.4(SDHD):c.315-32T>C	rs4151637	0.11444
NM_003002.4(SDHD):c.170-29A>G	rs9919624	0.11431
NM_003002.4(SDHD):c.204C>T (p.Ser68=)	rs9919552	0.11428
NM_003002.4(SDHD):c.34G>A (p.Gly12Ser)	rs34677591	0.00706
NM_005401.5(PTPN14):c.929+24del	rs11322819

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