List of variants in gene IFT122 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_052989.3(IFT122):c.1908T>C (p.Ile636=)	rs139722192	0.00334
NM_052989.3(IFT122):c.3432C>T (p.Ile1144=)	rs149884307	0.00277
NM_052989.3(IFT122):c.2294A>C (p.Lys765Thr)	rs146026277	0.00212
NM_052989.3(IFT122):c.273-331C>A	rs116196975	0.00187
NM_052989.3(IFT122):c.617T>C (p.Ile206Thr)	rs59912693	0.00184
NM_052989.3(IFT122):c.825G>T (p.Lys275Asn)	rs117517364	0.00095
NM_052989.3(IFT122):c.1026C>T (p.Asp342=)	rs79187669	0.00075
NM_052989.3(IFT122):c.3533G>A (p.Arg1178His)	rs149029829	0.00024
NM_052989.3(IFT122):c.1851+5C>T	rs375595062	0.00001
NM_052989.3(IFT122):c.1852-22T>C
NM_052989.3(IFT122):c.1950C>T (p.Ala650=)
NM_052989.3(IFT122):c.1959G>A (p.Ala653=)
NM_052989.3(IFT122):c.2301C>T (p.Ala767=)
NM_052989.3(IFT122):c.273-417del	rs201674500
NM_052989.3(IFT122):c.3195G>A (p.Pro1065=)

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