List of variants in gene TMEM231 reported as benign for Meckel syndrome

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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.582+17T>A	rs2738801	0.27293
NM_001077418.3(TMEM231):c.-6G>C	rs3743602	0.21908
NM_001077418.3(TMEM231):c.16C>G (p.Leu6Val)	rs3743601	0.10494
NM_001077418.3(TMEM231):c.813G>A (p.Val271=)	rs2242406	0.08287
NM_001077418.3(TMEM231):c.582+8C>G	rs144252983	0.02257
NM_001077418.3(TMEM231):c.582+3A>G	rs114290622	0.01823
NM_001077418.3(TMEM231):c.177G>C (p.Pro59=)	rs78196225	0.01307
NM_001077418.3(TMEM231):c.498G>A (p.Pro166=)	rs201636741	0.00468
NM_001077418.3(TMEM231):c.891G>A (p.Val297=)	rs149888762	0.00375
NM_001077418.3(TMEM231):c.91G>A (p.Ala31Thr)	rs202215735	0.00182
NM_001077418.3(TMEM231):c.804C>T (p.Phe268=)	rs149118721	0.00144
NM_001077418.3(TMEM231):c.900T>C (p.Ile300=)	rs199628375	0.00089
NM_001077418.3(TMEM231):c.471G>A (p.Ala157=)	rs375273015	0.00077
NM_001077418.3(TMEM231):c.376C>T (p.Leu126=)	rs557695110	0.00007
NC_000016.9:g.(?_75573892)_(75575373_?)dup
NC_000016.9:g.(?_75573892)_(75576601_?)dup

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