List of variants in gene combination LOC130004614, SUFU studied for Medulloblastoma; Familial meningioma; Joubert syndrome 32; Basal cell nevus syndrome 2

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_016169.4(SUFU):c.12G>A (p.Leu4=)	rs189234140	0.00425
NM_016169.4(SUFU):c.26C>T (p.Ala9Val)	rs775491374	0.00001
NM_016169.4(SUFU):c.32G>A (p.Gly11Asp)	rs1227379293	0.00001
NM_016169.4(SUFU):c.31G>C (p.Gly11Arg)	rs1322807658
NM_016169.4(SUFU):c.37A>C (p.Thr13Pro)	rs1456048322
NM_016169.4(SUFU):c.37_42del (p.Thr13_Ala14del)	rs1589969829
NM_016169.4(SUFU):c.9G>C (p.Glu3Asp)

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