List of variants in gene TUBA8 reported as benign for not provided

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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: 25

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HGVS	dbSNP	gnomAD frequency
NM_018943.3(TUBA8):c.376-56G>T	rs2234329	0.11122
NM_018943.3(TUBA8):c.1056+53G>A	rs361776	0.10627
NM_018943.3(TUBA8):c.375+20_375+22del	rs71703459	0.07113
NM_018943.3(TUBA8):c.1057-7C>T	rs2234338	0.06275
NM_018943.3(TUBA8):c.897C>T (p.Asn299=)	rs362203	0.06153
NM_018943.3(TUBA8):c.376-75G>A	rs362195	0.05559
NM_018943.3(TUBA8):c.375+235A>T	rs9604830	0.03092
NM_018943.3(TUBA8):c.226+81C>T	rs2234325	0.02996
NM_018943.3(TUBA8):c.1057-141_1057-128del	rs58525003	0.02325
NM_018943.3(TUBA8):c.816C>T (p.Tyr272=)	rs2234332	0.01553
NM_018943.3(TUBA8):c.383C>T (p.Ala128Val)	rs2234331	0.00762
NM_018943.3(TUBA8):c.250C>T (p.Arg84Cys)	rs115847686	0.00577
NM_018943.3(TUBA8):c.748G>A (p.Val250Met)	rs145621219	0.00314
NM_018943.3(TUBA8):c.1173C>T (p.Leu391=)	rs201432541	0.00166
NM_018943.3(TUBA8):c.324C>T (p.Tyr108=)	rs2234327	0.00115
NM_018943.3(TUBA8):c.1080G>A (p.Pro360=)	rs145407514	0.00102
NM_018943.3(TUBA8):c.902A>G (p.Gln301Arg)	rs2234333	0.00028
NM_018943.3(TUBA8):c.251G>A (p.Arg84His)	rs137904008	0.00021
NM_018943.3(TUBA8):c.570C>T (p.Thr190=)	rs141040298	0.00021
NC_000022.11:g.18110514G>A	rs2234321
NM_018943.3(TUBA8):c.1057-237del	rs362251
NM_018943.3(TUBA8):c.1057-238_1057-237del	rs362251
NM_018943.3(TUBA8):c.226+22dup
NM_018943.3(TUBA8):c.376-302G>T	rs467262
NM_018943.3(TUBA8):c.4-5del	rs2123699667

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