List of variants in gene TINF2 reported 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
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001099274.3(TINF2):c.1092G>A (p.Leu364=)	rs184422577	0.00410
NM_001099274.3(TINF2):c.1236C>T (p.Asn412=)	rs117234138	0.00329
NM_001099274.3(TINF2):c.771C>T (p.His257=)	rs75124018	0.00106
NM_001099274.3(TINF2):c.734C>A (p.Ser245Tyr)	rs142777869	0.00034
NM_001099274.3(TINF2):c.51G>C (p.Ala17=)	rs757222975	0.00003
NM_001099274.3(TINF2):c.302A>G (p.Lys101Arg)	rs1375036989	0.00002
NM_001099274.3(TINF2):c.984dup (p.Lys329Ter)	rs903141690	0.00001
NM_001099274.3(TINF2):c.1044del (p.Ala349fs)
NM_001099274.3(TINF2):c.193-1G>A
NM_001099274.3(TINF2):c.623C>G (p.Ser208Ter)
NM_001099274.3(TINF2):c.865C>T (p.Pro289Ser)	rs1555304055
NM_001099274.3(TINF2):c.934T>C (p.Tyr312His)

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