List of variants in gene TMEM231 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_001077418.3(TMEM231):c.928T>G (p.Leu310Val)	rs182008317	0.00181
NM_001077418.3(TMEM231):c.-40C>G	rs114889548	0.00177
NM_001077418.3(TMEM231):c.804C>T (p.Phe268=)	rs149118721	0.00144
NM_001077418.3(TMEM231):c.710G>C (p.Arg237Thr)	rs199813223	0.00141
NM_001077418.3(TMEM231):c.719A>G (p.Asp240Gly)	rs146210288	0.00138
NM_001077418.3(TMEM231):c.583-20A>T	rs375984875	0.00128
NM_001077418.3(TMEM231):c.-15C>T	rs138060715	0.00092
NM_001077418.3(TMEM231):c.129C>T (p.Phe43=)	rs377440297	0.00058
NM_001077418.3(TMEM231):c.79C>T (p.Leu27=)	rs370607340	0.00026
NM_001077418.3(TMEM231):c.583-9G>A	rs371734111	0.00011
NM_001077418.3(TMEM231):c.798A>G (p.Val266=)	rs772364535	0.00009
NM_001077418.3(TMEM231):c.624C>T (p.Tyr208=)	rs368594302	0.00007
NM_001077418.3(TMEM231):c.582+6A>G	rs376300743	0.00006
NM_001077418.3(TMEM231):c.771-4A>C	rs199768195	0.00003
NM_001077418.3(TMEM231):c.771-6C>A	rs1160382019	0.00001
NM_001077416.2(TMEM231):c.-2C>A

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