List of variants in gene KBTBD13 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001101362.3(KBTBD13):c.1077A>G (p.Gly359=)	rs199526404	0.00224
NM_001101362.3(KBTBD13):c.214C>T (p.Leu72=)	rs550537101	0.00205
NM_001101362.3(KBTBD13):c.188A>T (p.Gln63Leu)	rs202004658	0.00175
NM_001101362.3(KBTBD13):c.815T>A (p.Ile272Asn)	rs558291810	0.00056
NM_001101362.3(KBTBD13):c.795C>T (p.Gly265=)	rs577503698	0.00038
NM_001101362.3(KBTBD13):c.205C>T (p.Arg69Trp)	rs530722554	0.00034
NM_001101362.3(KBTBD13):c.880C>G (p.Pro294Ala)	rs560695692	0.00023
NM_001101362.3(KBTBD13):c.876G>A (p.Pro292=)	rs543905658	0.00006
NM_001101362.3(KBTBD13):c.276G>C (p.Ala92=)	rs566529505	0.00004
NM_001101362.3(KBTBD13):c.861C>T (p.Phe287=)	rs777259450	0.00003
NM_001101362.3(KBTBD13):c.1341T>C (p.Ala447=)	rs1298809117	0.00001
NM_001101362.3(KBTBD13):c.295C>T (p.His99Tyr)	rs886038411	0.00001
NM_001101362.3(KBTBD13):c.-3G>A
NM_001101362.3(KBTBD13):c.361G>C (p.Val121Leu)	rs201466173

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