ClinVar Miner

List of variants in gene TNC reported by Neuberg Centre For Genomic Medicine, NCGM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002160.4(TNC):c.1973C>A (p.Pro658His)	rs1209292182
NM_002160.4(TNC):c.3442A>G (p.Ile1148Val)
NM_002160.4(TNC):c.848T>C (p.Leu283Pro)

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