List of variants in gene IFT122 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: 11

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HGVS	dbSNP	gnomAD frequency
NM_052989.3(IFT122):c.1273C>T (p.Arg425Trp)	rs61744639	0.00451
NM_052989.3(IFT122):c.321A>G (p.Gln107=)	rs138793724	0.00299
NM_052989.3(IFT122):c.3129C>T (p.Arg1043=)	rs76881473	0.00206
NM_052989.3(IFT122):c.1103G>A (p.Ser368Asn)	rs150550701	0.00133
NM_052989.3(IFT122):c.3487T>A (p.Phe1163Ile)	rs200606803	0.00057
NM_052989.3(IFT122):c.3046C>T (p.Arg1016Trp)	rs776052135	0.00005
NM_052989.3(IFT122):c.273-239A>G	rs1362422868	0.00001
NM_052989.3(IFT122):c.1171G>C (p.Val391Leu)
NM_052989.3(IFT122):c.1437C>T (p.Ile479=)
NM_052989.3(IFT122):c.1883A>C (p.Lys628Thr)
NM_052989.3(IFT122):c.3501G>A (p.Val1167=)

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