List of variants in gene SUFU reported as benign by Ambry Genetics

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.1299T>C (p.Ile433=)	rs17114803	0.14628
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser)	rs34135067	0.00646
NM_016169.4(SUFU):c.1291T>C (p.Leu431=)	rs141950577	0.00487
NM_016169.4(SUFU):c.210T>C (p.Tyr70=)	rs35166585	0.00430
NM_016169.4(SUFU):c.412G>A (p.Ala138Thr)	rs34406289	0.00078
NM_016169.4(SUFU):c.1445C>T (p.Pro482Leu)	rs765358771	0.00020
NM_016169.4(SUFU):c.1308C>T (p.Thr436=)	rs142029957	0.00018
NM_016169.4(SUFU):c.880G>A (p.Gly294Ser)	rs143807689	0.00017
NM_016169.4(SUFU):c.1058C>T (p.Thr353Met)	rs137880855	0.00014
NM_016169.4(SUFU):c.1028G>A (p.Arg343His)	rs79299301	0.00008
NM_016169.4(SUFU):c.625C>T (p.His209Tyr)	rs770678862	0.00007
NM_016169.4(SUFU):c.1105G>A (p.Val369Ile)	rs149449923	0.00006
NM_016169.4(SUFU):c.1059G>A (p.Thr353=)	rs780683814	0.00005
NM_016169.4(SUFU):c.1157+3G>A	rs764861812	0.00003
NM_016169.4(SUFU):c.1379A>G (p.Lys460Arg)	rs778125780	0.00001

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