List of variants in gene SUGCT 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001193313.2(SUGCT):c.1206G>C (p.Pro402=)	rs2010706	0.33644
NM_001193313.2(SUGCT):c.630G>A (p.Leu210=)	rs12669315	0.29439
NM_001193313.2(SUGCT):c.708A>G (p.Leu236=)	rs4637704	0.28622
NM_001193313.2(SUGCT):c.227-16A>T	rs78060149	0.12444
NM_001193313.2(SUGCT):c.485-6T>C	rs76667176	0.06983
NM_001193313.2(SUGCT):c.889-7C>A	rs6960628	0.04276
NM_001193313.2(SUGCT):c.1226C>T (p.Thr409Met)	rs192063213	0.00672
NM_001193313.2(SUGCT):c.733T>C (p.Ser245Pro)	rs779940170	0.00010
NM_001193313.2(SUGCT):c.313-16A>T	rs10236765
NM_001193313.2(SUGCT):c.313-30AT[7]	rs563908901
NM_001193313.2(SUGCT):c.313-30AT[9]	rs563908901

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