List of variants in gene TNFRSF1A reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.935G>A (p.Arg312Lys)	rs200900510	0.00113
NM_001065.4(TNFRSF1A):c.1328G>T (p.Gly443Val)	rs201062001	0.00011
NM_001065.4(TNFRSF1A):c.334G>A (p.Val112Met)	rs201753543	0.00007
NM_001065.4(TNFRSF1A):c.1038C>G (p.His346Gln)	rs201994938	0.00003
NM_001065.4(TNFRSF1A):c.1256A>G (p.Glu419Gly)	rs1454639907	0.00001
NM_001065.4(TNFRSF1A):c.269C>T (p.Thr90Ile)	rs34751757	0.00001
NM_001065.4(TNFRSF1A):c.323-3C>G	rs1328399119	0.00001
NM_001065.4(TNFRSF1A):c.482A>G (p.Lys161Arg)	rs578112440	0.00001
NM_001065.4(TNFRSF1A):c.914C>G (p.Pro305Arg)	rs1344445194	0.00001
NM_001065.4(TNFRSF1A):c.1217C>T (p.Thr406Ile)	rs1592043182
NM_001065.4(TNFRSF1A):c.1246G>A (p.Ala416Thr)
NM_001065.4(TNFRSF1A):c.212A>T (p.Asp71Val)	rs1592047919
NM_001065.4(TNFRSF1A):c.92T>G (p.Val31Gly)	rs763940329

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