List of variants in gene TRAPPC12 reported as pathogenic for not provided

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

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
GRCh37/hg19 2p25.3(chr2:3385474-3418641)x1
NC_000002.11:g.(?_3391395)_(3428454_?)del
NM_016030.6(TRAPPC12):c.1127C>G (p.Ser376Ter)
NM_016030.6(TRAPPC12):c.1677+5G>A

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