List of variants in gene SUFU reported as benign for not specified

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.*20T>G	rs4917980	0.99823
NM_016169.4(SUFU):c.1365+19T>C	rs12414407	0.68304
NM_016169.4(SUFU):c.182+16C>T	rs2274351	0.46492
NM_016169.4(SUFU):c.1299T>C (p.Ile433=)	rs17114803	0.15159
NM_016169.4(SUFU):c.1023-23C>G	rs117407459	0.01067
NM_016169.4(SUFU):c.1018G>T (p.Ala340Ser)	rs34135067	0.00629
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.1308C>T (p.Thr436=)	rs142029957	0.00025
NM_016169.4(SUFU):c.1245C>T (p.Gly415=)	rs144158469	0.00011
NM_016169.4(SUFU):c.855C>T (p.Asp285=)	rs200206997	0.00004

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