List of variants reported as likely benign for Medulloblastoma

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Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.*1675G>A	rs41287466	0.03346
NM_016169.4(SUFU):c.*3086A>G	rs73342651	0.01014
NM_016169.4(SUFU):c.*1672A>G	rs117196884	0.01007
NM_016169.4(SUFU):c.*205G>A	rs115428806	0.00961
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser)	rs34135067	0.00646
NM_016169.4(SUFU):c.*3290C>G	rs112808377	0.00612
NM_016169.4(SUFU):c.-33C>T	rs201649559	0.00587
NM_016169.4(SUFU):c.1291T>C (p.Leu431=)	rs141950577	0.00487
NM_016169.4(SUFU):c.*2157C>T	rs181690906	0.00474
NM_016169.4(SUFU):c.210T>C (p.Tyr70=)	rs35166585	0.00430
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NM_016169.4(SUFU):c.*2720C>T	rs41287468	0.00417
NM_016169.4(SUFU):c.*505T>G	rs116570216	0.00412
NM_016169.4(SUFU):c.*2172G>A	rs540579682	0.00367
NM_016169.4(SUFU):c.*3268G>C	rs150653416	0.00308
NM_016169.4(SUFU):c.*61G>A	rs184505927	0.00249
NM_016169.4(SUFU):c.910+14C>T	rs202247757	0.00139
NM_016169.4(SUFU):c.600C>T (p.Ile200=)	rs149513330	0.00116
NM_016169.4(SUFU):c.*2140G>T	rs543282016	0.00019
NM_016169.4(SUFU):c.1308C>T (p.Thr436=)	rs142029957	0.00018
NM_016169.4(SUFU):c.*2150G>A	rs561461171
NM_016169.4(SUFU):c.*742G>A	rs142145337

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