List of variants in gene CSPP1 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: 8

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HGVS	dbSNP	gnomAD frequency
NM_001382391.1(CSPP1):c.773G>A (p.Arg258Lys)	rs199901120	0.00019
NM_001382391.1(CSPP1):c.484-4A>G	rs142440392	0.00004
NM_001382391.1(CSPP1):c.1645C>G (p.Pro549Ala)	rs754153035	0.00001
NM_001382391.1(CSPP1):c.1708G>A (p.Gly570Arg)	rs2129554180
NM_001382391.1(CSPP1):c.2504G>A (p.Cys835Tyr)
NM_001382391.1(CSPP1):c.2516A>G (p.Asn839Ser)
NM_001382391.1(CSPP1):c.2675C>T (p.Pro892Leu)
NM_001382391.1(CSPP1):c.676T>A (p.Leu226Ile)

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