ClinVar Miner

List of variants in gene combination LOC130004614, SUFU reported by Sema4, Sema4

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.50C>T (p.Ala17Val)	rs12780580	0.00023
NM_016169.4(SUFU):c.6G>T (p.Ala2=)	rs746555296	0.00021
NM_016169.4(SUFU):c.27C>A (p.Ala9=)	rs1244167364
NM_016169.4(SUFU):c.31G>C (p.Gly11Arg)	rs1322807658

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