List of variants in gene SUFU reported as uncertain significance by Sema4, Sema4

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.1084C>T (p.Arg362Cys)	rs36049457	0.00039
NM_016169.4(SUFU):c.839G>A (p.Arg280Gln)	rs145704867	0.00017
NM_016169.4(SUFU):c.880G>A (p.Gly294Ser)	rs143807689	0.00017
NM_016169.4(SUFU):c.625C>T (p.His209Tyr)	rs770678862	0.00007
NM_016169.4(SUFU):c.911-7G>A	rs558661774	0.00006
NM_016169.4(SUFU):c.275G>C (p.Ser92Thr)	rs746322193	0.00002
NM_016169.4(SUFU):c.1016G>A (p.Arg339Gln)	rs369910221	0.00001
NM_016169.4(SUFU):c.107C>T (p.Ala36Val)	rs566714720	0.00001
NM_016169.4(SUFU):c.1379A>G (p.Lys460Arg)	rs778125780	0.00001
NM_016169.4(SUFU):c.894G>T (p.Arg298=)	rs372636246	0.00001
NM_016169.4(SUFU):c.1061C>G (p.Ala354Gly)	rs1554854572
NM_016169.4(SUFU):c.118G>A (p.Glu40Lys)	rs2135598310
NM_016169.4(SUFU):c.868A>G (p.Ser290Gly)	rs1406131774

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