List of variants in gene TINF2 reported as uncertain significance for perceptual disorders

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_001099274.3(TINF2):c.371C>T (p.Ala124Val)	rs369712095	0.00013
NM_001099274.3(TINF2):c.403C>T (p.Leu135Phe)	rs199740488	0.00012
NM_001099274.3(TINF2):c.1030C>T (p.Pro344Ser)	rs200454893	0.00010
NM_001099274.3(TINF2):c.1307C>T (p.Ala436Val)	rs369249473	0.00008
NM_001099274.3(TINF2):c.-277C>G	rs886050435	0.00006
NM_001099274.3(TINF2):c.936C>A (p.Tyr312Ter)	rs201677741	0.00006
NM_001099274.3(TINF2):c.30A>G (p.Ala10=)	rs779819186	0.00004
NM_001099274.3(TINF2):c.767G>A (p.Arg256Gln)	rs779837822	0.00004
NM_001099274.3(TINF2):c.278T>C (p.Ile93Thr)	rs762140055	0.00003
NM_001099274.3(TINF2):c.1084G>C (p.Asp362His)	rs371044766	0.00002
NM_001099274.3(TINF2):c.1076G>A (p.Cys359Tyr)	rs368350757	0.00001
NM_001099274.3(TINF2):c.1139C>T (p.Pro380Leu)	rs201422008	0.00001
NM_001099274.3(TINF2):c.622T>C (p.Ser208Pro)	rs377436580	0.00001
NM_001099274.3(TINF2):c.679C>T (p.Leu227Phe)	rs754706260	0.00001
NM_001099274.3(TINF2):c.802G>C (p.Val268Leu)	rs369926102	0.00001
NM_001099274.3(TINF2):c.932T>C (p.Ile311Thr)	rs757221051	0.00001
NM_001099274.3(TINF2):c.*53G>A	rs886050429
NM_001099274.3(TINF2):c.1061+4_1061+7del
NM_001099274.3(TINF2):c.1074T>C (p.Asp358=)	rs886050430
NM_001099274.3(TINF2):c.1237_1240del (p.Tyr413fs)
NM_001099274.3(TINF2):c.1285C>A (p.Leu429Ile)	rs780647966
NM_001099274.3(TINF2):c.1338_1339del (p.Asp446fs)
NM_001099274.3(TINF2):c.268T>G (p.Ser90Ala)
NM_001099274.3(TINF2):c.400-5del	rs769170035
NM_001099274.3(TINF2):c.494_502del (p.Pro165_Ala167del)	rs747496593
NM_001099274.3(TINF2):c.517G>A (p.Val173Met)	rs2040569011
NM_001099274.3(TINF2):c.607T>C (p.Cys203Arg)	rs2040562236
NM_001099274.3(TINF2):c.682C>T (p.His228Tyr)	rs886050431
NM_001099274.3(TINF2):c.962G>C (p.Arg321Thr)
NM_012461.3(TINF2):c.-316G>A	rs886050436

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