List of variants in gene TUSC2 reported as uncertain significance by Ambry Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_007275.3(TUSC2):c.293G>A (p.Arg98His)	rs1553717365	0.00001
NM_007275.3(TUSC2):c.125C>T (p.Pro42Leu)
NM_007275.3(TUSC2):c.16T>C (p.Ser6Pro)	rs2470887389
NM_007275.3(TUSC2):c.17C>T (p.Ser6Phe)	rs2470887385
NM_007275.3(TUSC2):c.25C>T (p.Arg9Trp)	rs1553717649
NM_007275.3(TUSC2):c.292C>T (p.Arg98Cys)
NM_007275.3(TUSC2):c.301G>A (p.Val101Met)	rs140522021

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