ClinVar Miner

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

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_001039213.4(CEACAM16):c.114G>A (p.Thr38=) rs894189 0.12083
NM_001039213.4(CEACAM16):c.941-14C>T rs10426475 0.05915
NM_001039213.4(CEACAM16):c.1268-13A>G rs143934888 0.03594
NM_001039213.4(CEACAM16):c.1278A>G (p.Ter426=) rs146757817 0.01185
NM_001039213.4(CEACAM16):c.234C>T (p.Gly78=) rs73568059 0.00319
NM_001039213.4(CEACAM16):c.738G>A (p.Thr246=) rs199779296 0.00300
NM_001039213.4(CEACAM16):c.1203C>T (p.Tyr401=) rs61744494 0.00286
NM_001039213.4(CEACAM16):c.43T>C (p.Phe15Leu) rs114907619 0.00283
NM_001039213.4(CEACAM16):c.352G>A (p.Glu118Lys) rs183860695 0.00221
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.539C>T (p.Ser180Phe) rs59028589 0.00032
NM_001039213.4(CEACAM16):c.51T>C (p.Asn17=) rs202230938 0.00004
NM_001039213.4(CEACAM16):c.1215= (p.Thr405=) rs61744497

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