List of variants in gene SUMF1 reported by Mayo Clinic Laboratories, Mayo Clinic

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_182760.4(SUMF1):c.1116T>C (p.Thr372=)	rs2633852	0.66322
NM_182760.4(SUMF1):c.445-22T>C	rs711634	0.03328
NM_182760.4(SUMF1):c.602+13C>T	rs80204284	0.01808
NM_182760.4(SUMF1):c.1015-22C>T	rs77991674	0.01138
NM_182760.4(SUMF1):c.-9C>T	rs148200251	0.00803
NM_182760.4(SUMF1):c.664G>C (p.Gly222Arg)	rs137917233	0.00180
NM_182760.4(SUMF1):c.875A>G (p.Tyr292Cys)	rs148841895	0.00014
NM_182760.4(SUMF1):c.463T>C (p.Ser155Pro)	rs137852850	0.00009
NM_182760.4(SUMF1):c.726-16G>T	rs999626972	0.00001
NM_182760.4(SUMF1):c.10_11delinsGT	rs71623163
NM_182760.4(SUMF1):c.*11A>T	rs2633851
NM_182760.4(SUMF1):c.37T>C (p.Cys13Arg)

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