List of variants in gene CEACAM16 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_001039213.4(CEACAM16):c.519C>T (p.Val173=)	rs114645388	0.00086
NM_001039213.4(CEACAM16):c.999C>T (p.Asp333=)	rs200767877	0.00075
NM_001039213.4(CEACAM16):c.1125G>A (p.Ala375=)	rs373050209	0.00031
NM_001039213.4(CEACAM16):c.520G>A (p.Ala174Thr)	rs750153629	0.00019
NM_001039213.4(CEACAM16):c.527G>A (p.Arg176His)	rs746541677	0.00011
NM_001039213.4(CEACAM16):c.1045G>A (p.Ala349Thr)	rs187740201	0.00006
NM_001039213.4(CEACAM16):c.546C>T (p.Asp182=)	rs747829770	0.00006
NM_001039213.4(CEACAM16):c.565C>T (p.His189Tyr)	rs370890913	0.00005
NM_001039213.4(CEACAM16):c.1104A>G (p.Gly368=)	rs750455256	0.00003
NM_001039213.4(CEACAM16):c.517G>A (p.Val173Ile)	rs756280582	0.00002
NM_001039213.4(CEACAM16):c.359G>C (p.Gly120Ala)	rs979461820	0.00001
NM_001039213.4(CEACAM16):c.*4C>A	rs199656542
NM_001039213.4(CEACAM16):c.1249G>C (p.Val417Leu)	rs199597608
NM_001039213.4(CEACAM16):c.246G>A (p.Thr82=)	rs761814983
NM_001039213.4(CEACAM16):c.941-8C>T	rs876657441

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