List of variants in gene SUFU reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
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.910+14C>T	rs202247757	0.00133
NM_016169.4(SUFU):c.412G>A (p.Ala138Thr)	rs34406289	0.00072
NM_016169.4(SUFU):c.318-17C>A	rs201198734	0.00029
NM_016169.4(SUFU):c.1308C>T (p.Thr436=)	rs142029957	0.00025
NM_016169.4(SUFU):c.839G>A (p.Arg280Gln)	rs145704867	0.00017
NM_016169.4(SUFU):c.1245C>T (p.Gly415=)	rs144158469	0.00011
NM_016169.4(SUFU):c.1028G>A (p.Arg343His)	rs79299301	0.00008
NM_016169.4(SUFU):c.879C>T (p.Ile293=)	rs370516021	0.00007
NM_016169.4(SUFU):c.183-4G>A	rs766044613	0.00005
NM_016169.4(SUFU):c.318-7C>G	rs751778806	0.00003
NM_016169.4(SUFU):c.474G>A (p.Gly158=)	rs375178556	0.00003
NM_016169.4(SUFU):c.1008C>T (p.Ala336=)	rs770049693	0.00002
NM_016169.4(SUFU):c.1446G>A (p.Pro482=)	rs761389038	0.00002
NM_016169.4(SUFU):c.671G>A (p.Arg224Gln)	rs199673680	0.00002
NM_016169.4(SUFU):c.1030A>C (p.Lys344Gln)	rs1590082116	0.00001
NM_016169.4(SUFU):c.1221G>A (p.Thr407=)	rs555064651	0.00001
NM_016169.4(SUFU):c.256G>A (p.Glu86Lys)	rs770989077	0.00001
NM_016169.4(SUFU):c.480T>C (p.His160=)	rs1308247295	0.00001
NM_016169.4(SUFU):c.730A>G (p.Ile244Val)	rs1378645161	0.00001
NM_016169.4(SUFU):c.910+8C>G	rs1159461161	0.00001
NM_016169.4(SUFU):c.933C>A (p.Thr311=)	rs767071744	0.00001
NM_016169.4(SUFU):c.*6G>A	rs375366321
NM_016169.4(SUFU):c.1008_1012delinsTGAGGC (p.His337fs)	rs2545101102
NM_016169.4(SUFU):c.1188A>C (p.Thr396=)	rs1418070936
NM_016169.4(SUFU):c.176A>G (p.Lys59Arg)	rs2544831922
NM_016169.4(SUFU):c.317+3G>A	rs2135621016
NM_016169.4(SUFU):c.895_896insTGTGT (p.Arg299fs)	rs1564698850

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