List of variants in gene SUMF1 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: 17

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HGVS	dbSNP	gnomAD frequency
NM_182760.4(SUMF1):c.602+50G>A	rs711666	0.90409
NM_182760.4(SUMF1):c.1116T>C (p.Thr372=)	rs2633852	0.66322
NM_182760.4(SUMF1):c.*10A>G	rs35083095	0.42363
NM_182760.4(SUMF1):c.445-22T>C	rs711634	0.03328
NM_182760.4(SUMF1):c.444+27A>G	rs56662447	0.00821
NM_182760.4(SUMF1):c.841-14G>A	rs9852367	0.00720
NM_182760.4(SUMF1):c.1077G>A (p.Ser359=)	rs140751492	0.00285
NM_182760.4(SUMF1):c.664G>C (p.Gly222Arg)	rs137917233	0.00180
NM_182760.4(SUMF1):c.722A>G (p.Asn241Ser)	rs138045351	0.00080
NM_182760.4(SUMF1):c.528T>C (p.Ala176=)	rs138269123	0.00009
NM_182760.4(SUMF1):c.445-16C>T	rs373525151	0.00008
NM_182760.4(SUMF1):c.726-10C>T	rs1320187586	0.00002
NM_182760.4(SUMF1):c.520-48A>G	rs770383117	0.00001
NM_182760.4(SUMF1):c.*11A>T	rs2633851
NM_182760.4(SUMF1):c.841-15T>G	rs886038754
NM_182760.4(SUMF1):c.955-2A>G
NM_182760.4(SUMF1):c.95C>T (p.Ala32Val)	rs374677940

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