List of variants in gene TRAPPC9 reported as benign for Intellectual disability, autosomal recessive 13

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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: 11

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HGVS	dbSNP	gnomAD frequency
NM_001160372.4(TRAPPC9):c.2557-13T>A	rs9792174	0.57247
NM_001160372.4(TRAPPC9):c.207T>C (p.Gly69=)	rs3735801	0.55959
NM_001160372.4(TRAPPC9):c.288T>C (p.Phe96=)	rs3735802	0.55845
NM_001160372.4(TRAPPC9):c.411C>T (p.Asn137=)	rs3735803	0.45974
NM_001160372.4(TRAPPC9):c.1134+21A>G	rs3779658	0.27421
NM_001160372.4(TRAPPC9):c.1692C>T (p.Asn564=)	rs12549048	0.23649
NM_001160372.4(TRAPPC9):c.2431+7G>A	rs11166964	0.10663
NM_031466.8(TRAPPC9):c.-11+10G>A	rs117206975	0.01054
NM_001160372.4(TRAPPC9):c.7G>A (p.Val3Ile)	rs76033442	0.00462
NM_001160372.4(TRAPPC9):c.731-31_731-11del	rs11267571
NM_031466.8(TRAPPC9):c.-129_-109dup	rs367682297

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