List of variants in gene combination LOC126807238, TRAPPC11 reported as benign for hereditary skeletal muscle disorder

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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: 5

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HGVS	dbSNP	gnomAD frequency
NM_021942.6(TRAPPC11):c.2370C>T (p.Thr790=)	rs4862234	0.25098
NM_021942.6(TRAPPC11):c.2434A>C (p.Thr812Pro)	rs62358032	0.07525
NM_021942.6(TRAPPC11):c.2483T>C (p.Val828Ala)	rs75176151	0.00765
NM_021942.6(TRAPPC11):c.2461G>A (p.Ala821Thr)	rs114471872	0.00448
NM_021942.6(TRAPPC11):c.2388A>C (p.Gly796=)	rs151021715	0.00089

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