List of variants in gene CEACAM16 reported as pathogenic 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
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.703C>T (p.Arg235Cys)	rs746164064	0.00004
NM_001039213.4(CEACAM16):c.763A>G (p.Arg255Gly)	rs1347137461	0.00001
NM_001039213.4(CEACAM16):c.37G>T (p.Ala13Ser)	rs1198256157
NM_001039213.4(CEACAM16):c.418A>C (p.Thr140Pro)	rs387907149
NM_001039213.4(CEACAM16):c.436C>T (p.Arg146Ter)
NM_001039213.4(CEACAM16):c.505G>A (p.Gly169Arg)	rs876661405
NM_001039213.4(CEACAM16):c.662-1G>C	rs1568528171

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