List of variants in gene MASTL reported as benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001172303.3(MASTL):c.812-28G>A	rs788238	0.99319
NM_001172303.3(MASTL):c.-27T>C	rs7907981	0.79017
NM_001172303.3(MASTL):c.-28C>A	rs7919803	0.60854
NM_001172303.3(MASTL):c.1782C>T (p.Ile594=)	rs1981296	0.60781
NM_001172303.3(MASTL):c.660+12A>T	rs7068375	0.60773
NM_001172303.3(MASTL):c.465-32G>C	rs12572707	0.07219
NM_001172303.3(MASTL):c.1858C>G (p.Pro620Ala)	rs3802526	0.06970
NM_001172303.3(MASTL):c.186+37C>T	rs41282218	0.05796
NM_001172303.3(MASTL):c.2139G>A (p.Gln713=)	rs41282228	0.01126
NM_001172303.3(MASTL):c.477G>A (p.Pro159=)	rs56204835	0.00583
NM_001172303.3(MASTL):c.1010C>A (p.Thr337Lys)	rs36121140	0.00398
NM_001172303.3(MASTL):c.1930A>C (p.Lys644Gln)	rs140163549	0.00009
NM_001172303.3(MASTL):c.-12T>G	rs7907988

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