List of variants in gene CNNM4 studied for perceptual disorders

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: 14

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HGVS	dbSNP	gnomAD frequency
NM_020184.4(CNNM4):c.2130+5G>A	rs200517269	0.00024
NM_020184.4(CNNM4):c.91T>C (p.Trp31Arg)	rs760633483	0.00017
NM_020184.4(CNNM4):c.1690C>T (p.Gln564Ter)	rs80100937	0.00001
NM_020184.4(CNNM4):c.1195G>A (p.Glu399Lys)
NM_020184.4(CNNM4):c.1312dup (p.Leu438fs)
NM_020184.4(CNNM4):c.1555C>T (p.Arg519Ter)	rs1455470131
NM_020184.4(CNNM4):c.2147A>G (p.Tyr716Cys)
NM_020184.4(CNNM4):c.451T>C (p.Cys151Arg)
NM_020184.4(CNNM4):c.613_621delinsA (p.Gly205fs)	rs2078763986
NM_020184.4(CNNM4):c.648dup (p.Val217fs)	rs2078764558
NM_020184.4(CNNM4):c.731G>T (p.Cys244Phe)	rs1300890772
NM_020184.4(CNNM4):c.880C>T (p.His294Tyr)
NM_020184.4(CNNM4):c.947T>G (p.Leu316Arg)
NM_020184.4(CNNM4):c.9_55del (p.Val4fs)

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