List of variants in gene SNRNP200 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_014014.5(SNRNP200):c.46-7T>C	rs373701482	0.00022
NM_014014.5(SNRNP200):c.3130G>T (p.Val1044Leu)	rs755983089	0.00009
NM_014014.5(SNRNP200):c.4230C>T (p.Gly1410=)	rs747476940	0.00005
NM_014014.5(SNRNP200):c.3721C>T (p.Leu1241Phe)	rs1553440063	0.00001
NM_014014.5(SNRNP200):c.1348C>G (p.Leu450Val)
NM_014014.5(SNRNP200):c.1627C>T (p.Pro543Ser)	rs1057519143
NM_014014.5(SNRNP200):c.3859C>T (p.Arg1287Trp)	rs1004264460
NM_014014.5(SNRNP200):c.583A>G (p.Ile195Val)	rs1574001405
NM_014014.5(SNRNP200):c.767A>C (p.Lys256Thr)	rs1574000198

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