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

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.738G>A (p.Thr246=)	rs199779296	0.00300
NM_001039213.4(CEACAM16):c.95G>T (p.Ser32Ile)	rs186687142	0.00178
NM_001039213.4(CEACAM16):c.96C>T (p.Ser32=)	rs191552868	0.00178
NM_001039213.4(CEACAM16):c.508G>A (p.Ala170Thr)	rs200297676	0.00105
NM_001039213.4(CEACAM16):c.999C>T (p.Asp333=)	rs200767877	0.00075
NM_001039213.4(CEACAM16):c.885G>A (p.Ala295=)	rs374698222	0.00031
NM_001039213.4(CEACAM16):c.819C>T (p.Asn273=)	rs376207716	0.00017
NM_001039213.4(CEACAM16):c.108C>T (p.Asn36=)	rs201786853	0.00004
NM_001039213.4(CEACAM16):c.780C>T (p.Pro260=)	rs375711025	0.00001
NM_001039213.4(CEACAM16):c.219C>T (p.Gly73=)	rs534225927
NM_001039213.4(CEACAM16):c.986C>T (p.Thr329Met)

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