List of variants in gene TTLL5 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_015072.5(TTLL5):c.2891G>A (p.Arg964Gln)	rs142169707	0.00269
NM_015072.5(TTLL5):c.2603-3T>C	rs185326652	0.00175
NM_015072.5(TTLL5):c.670G>A (p.Val224Met)	rs17849666	0.00105
NM_015072.5(TTLL5):c.3785T>C (p.Leu1262Pro)	rs143635737	0.00009
NM_015072.5(TTLL5):c.1568C>T (p.Ala523Val)	rs1393819034	0.00003
NM_015072.5(TTLL5):c.1291C>T (p.Pro431Ser)	rs750993500	0.00002
NM_015072.5(TTLL5):c.741G>A (p.Arg247=)	rs765401548	0.00001
NM_015072.5(TTLL5):c.1624T>G (p.Tyr542Asp)	rs760056637
NM_015072.5(TTLL5):c.2016-3T>C	rs1566596891
NM_015072.5(TTLL5):c.338T>G (p.Leu113Arg)
NM_015072.5(TTLL5):c.940A>G (p.Met314Val)

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