List of variants in gene TNFRSF1A reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 18

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HGVS	dbSNP	gnomAD frequency
NM_001065.4(TNFRSF1A):c.194-14G>A	rs104895241	0.00016
NM_001065.4(TNFRSF1A):c.596T>C (p.Ile199Thr)	rs104895247	0.00011
NM_001065.4(TNFRSF1A):c.887G>C (p.Ser296Thr)	rs770324989	0.00009
NM_001065.4(TNFRSF1A):c.434A>G (p.Asn145Ser)	rs104895288	0.00005
NM_001065.4(TNFRSF1A):c.121G>C (p.Asp41His)	rs199882512	0.00002
NM_001065.4(TNFRSF1A):c.823C>T (p.Pro275Ser)	rs758118907	0.00002
NM_001065.4(TNFRSF1A):c.1329C>A (p.Gly443=)	rs756455040	0.00001
NM_001065.4(TNFRSF1A):c.323-3C>G	rs1328399119	0.00001
NM_001065.4(TNFRSF1A):c.370G>A (p.Val124Met)	rs104895278	0.00001
NM_001065.4(TNFRSF1A):c.785C>G (p.Thr262Ser)	rs199649416	0.00001
NM_001065.4(TNFRSF1A):c.997C>T (p.Pro333Ser)	rs1338161780	0.00001
NM_001065.4(TNFRSF1A):c.1049G>A (p.Ser350Asn)	rs1948012552
NM_001065.4(TNFRSF1A):c.1103C>A (p.Pro368Gln)
NM_001065.4(TNFRSF1A):c.1180C>A (p.Arg394Ser)
NM_001065.4(TNFRSF1A):c.1271T>C (p.Val424Ala)	rs982742726
NM_001065.4(TNFRSF1A):c.472+6C>T	rs104895277
NM_001065.4(TNFRSF1A):c.491C>T (p.Thr164Ile)	rs1948071442
NM_001065.4(TNFRSF1A):c.575C>A (p.Thr192Lys)

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