List of variants in gene TRAPPC12 reported as benign for multiple congenital anomalies/dysmorphic 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: 6

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HGVS	dbSNP	gnomAD frequency
NM_016030.6(TRAPPC12):c.681T>C (p.Phe227=)	rs10865541	0.62092
NM_016030.6(TRAPPC12):c.2181C>T (p.Phe727=)	rs6767	0.44208
NM_016030.6(TRAPPC12):c.1773G>C (p.Leu591=)	rs4971514	0.41612
NM_016030.6(TRAPPC12):c.901A>G (p.Ser301Gly)	rs11686212	0.39295
NM_016030.6(TRAPPC12):c.432C>T (p.Ala144=)	rs11127423	0.22847
NM_016030.6(TRAPPC12):c.1047+72_1047+73delinsCA

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