List of variants in gene SF3B1 reported as likely pathogenic for transitional cell carcinoma

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_012433.4(SF3B1):c.1873C>G (p.Arg625Gly)	rs775623976	0.00001
NM_012433.4(SF3B1):c.1873C>T (p.Arg625Cys)	rs775623976
NM_012433.4(SF3B1):c.1874G>A (p.Arg625His)	rs1057519961

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