List of variants in gene CTU2 reported as likely 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001012759.3(CTU2):c.1425A>G (p.Ser475=)	rs78212226	0.00243
NM_001012759.3(CTU2):c.1531G>A (p.Glu511Lys)	rs201215099	0.00226
NM_001012759.3(CTU2):c.424T>C (p.Phe142Leu)	rs148239801	0.00111
NM_001012759.3(CTU2):c.1298G>C (p.Cys433Ser)	rs142662688	0.00107
NM_001012759.3(CTU2):c.404C>G (p.Pro135Arg)	rs144903142	0.00092
NM_001012759.3(CTU2):c.611C>T (p.Pro204Leu)	rs141967170	0.00087
NM_001012759.3(CTU2):c.1226A>C (p.Gln409Pro)	rs150644843	0.00031
NM_001012759.3(CTU2):c.1153G>A (p.Gly385Ser)	rs200076111	0.00029
NM_001012759.3(CTU2):c.1098-9C>T	rs200518996	0.00028
NM_001012759.3(CTU2):c.474G>A (p.Ser158=)	rs759082825	0.00011
NM_001012759.3(CTU2):c.1160G>A (p.Arg387His)	rs551005079	0.00010
NM_001012759.3(CTU2):c.894C>T (p.His298=)	rs750272877	0.00006
NM_001012759.3(CTU2):c.1183C>T (p.Leu395=)	rs770038426	0.00001
NM_001012759.3(CTU2):c.387C>G (p.Thr129=)	rs745307187	0.00001
NM_001012759.3(CTU2):c.454-6C>T	rs551897407	0.00001
NM_001012759.3(CTU2):c.-3C>G	rs570424055
NM_001012759.3(CTU2):c.1201+7_1201+8del	rs770862024
NM_001012759.3(CTU2):c.1202-8G>A	rs376937218
NM_001012759.3(CTU2):c.1353-4G>A	rs372591571
NM_001012759.3(CTU2):c.1419+8C>T
NM_001012759.3(CTU2):c.223-7C>T	rs114994631
NM_001012759.3(CTU2):c.393C>T (p.Ala131=)	rs141146913
NM_001012759.3(CTU2):c.736C>A (p.Arg246=)	rs767710092
NM_001012759.3(CTU2):c.771C>G (p.His257Gln)	rs73262667

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