List of variants in gene CFAP410 reported by OMIM

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_004928.3(CFAP410):c.347C>T (p.Pro116Leu)	rs922930539	0.00003
NM_004928.3(CFAP410):c.319T>C (p.Tyr107His)	rs763623409	0.00002
NM_004928.3(CFAP410):c.331G>A (p.Val111Met)	rs555164150	0.00002
NM_004928.3(CFAP410):c.545+1G>A	rs778222701	0.00001
NM_004928.3(CFAP410):c.103del (p.Ile35fs)	rs1114167893
NM_004928.3(CFAP410):c.182G>A (p.Cys61Tyr)	rs1057518441
NM_004928.3(CFAP410):c.218G>C (p.Arg73Pro)	rs140451304
NM_004928.3(CFAP410):c.320A>G (p.Tyr107Cys)	rs1131690801
NM_004928.3(CFAP410):c.436_466del (p.Glu146fs)	rs746633371
NM_004928.3(CFAP410):c.643-23A>T	rs1131690800
NM_004928.3(CFAP410):c.671T>C (p.Leu224Pro)	rs1114167892

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