List of variants in gene KCND3 reported as uncertain significance by Ambry Genetics

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: 91

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.5C>A (p.Ala2Glu)	rs201340369	0.00066
NM_001378969.1(KCND3):c.641A>G (p.Lys214Arg)	rs142744204	0.00034
NM_001378969.1(KCND3):c.1702C>T (p.Arg568Cys)	rs144120746	0.00011
NM_001378969.1(KCND3):c.1703G>A (p.Arg568His)	rs200212002	0.00007
NM_001378969.1(KCND3):c.1348C>T (p.Leu450Phe)	rs150401343	0.00006
NM_001378969.1(KCND3):c.1889G>A (p.Arg630Gln)	rs774713377	0.00006
NM_001378969.1(KCND3):c.626C>T (p.Thr209Met)	rs771878661	0.00004
NM_001378969.1(KCND3):c.1960G>A (p.Ala654Thr)	rs774711788	0.00003
NM_001378969.1(KCND3):c.430G>A (p.Ala144Thr)	rs143933558	0.00003
NM_001378969.1(KCND3):c.1256G>A (p.Arg419His)	rs774338559	0.00002
NM_001378969.1(KCND3):c.1519-5C>T	rs376408039	0.00002
NM_001378969.1(KCND3):c.514G>A (p.Ala172Thr)	rs149488365	0.00002
NM_001378969.1(KCND3):c.1277G>A (p.Arg426His)	rs760274429	0.00001
NM_001378969.1(KCND3):c.1371G>A (p.Thr457=)	rs773858454	0.00001
NM_001378969.1(KCND3):c.1393A>G (p.Met465Val)	rs1245864814	0.00001
NM_001378969.1(KCND3):c.1427A>G (p.His476Arg)	rs1571626155	0.00001
NM_001378969.1(KCND3):c.1634C>T (p.Thr545Ile)	rs969494348	0.00001
NM_001378969.1(KCND3):c.1645C>T (p.Arg549Cys)	rs1294150954	0.00001
NM_001378969.1(KCND3):c.1648C>T (p.Arg550Cys)	rs778141653	0.00001
NM_001378969.1(KCND3):c.1724C>T (p.Thr575Met)	rs775768536	0.00001
NM_001378969.1(KCND3):c.1849A>G (p.Ile617Val)	rs948125814	0.00001
NM_001378969.1(KCND3):c.1861C>G (p.Pro621Ala)	rs752495973	0.00001
NM_001378969.1(KCND3):c.1879G>A (p.Gly627Arg)	rs372362132	0.00001
NM_001378969.1(KCND3):c.38G>A (p.Arg13Gln)	rs1339082402	0.00001
NM_001378969.1(KCND3):c.89C>A (p.Ala30Asp)	rs1307934269	0.00001
NM_001378969.1(KCND3):c.98A>T (p.Asp33Val)	rs760460512	0.00001
NM_001378969.1(KCND3):c.1070C>T (p.Ser357Leu)	rs867628133
NM_001378969.1(KCND3):c.1107-5C>A
NM_001378969.1(KCND3):c.1124C>T (p.Pro375Leu)	rs1664633885
NM_001378969.1(KCND3):c.1222C>T (p.Arg408Trp)
NM_001378969.1(KCND3):c.1223G>A (p.Arg408Gln)
NM_001378969.1(KCND3):c.1255C>T (p.Arg419Cys)
NM_001378969.1(KCND3):c.1291C>T (p.Arg431Cys)	rs777183510
NM_001378969.1(KCND3):c.1345C>T (p.Leu449Phe)
NM_001378969.1(KCND3):c.1372-4C>T
NM_001378969.1(KCND3):c.1376C>A (p.Thr459Asn)
NM_001378969.1(KCND3):c.1378C>G (p.Pro460Ala)
NM_001378969.1(KCND3):c.1417G>A (p.Glu473Lys)
NM_001378969.1(KCND3):c.1435C>A (p.Leu479Met)
NM_001378969.1(KCND3):c.1442A>G (p.His481Arg)
NM_001378969.1(KCND3):c.1485_1503del (p.Asp495fs)
NM_001378969.1(KCND3):c.1501C>T (p.Arg501Ter)
NM_001378969.1(KCND3):c.1505C>G (p.Thr502Ser)
NM_001378969.1(KCND3):c.1514T>A (p.Ile505Asn)
NM_001378969.1(KCND3):c.1535A>C (p.Asp512Ala)	rs1664166577
NM_001378969.1(KCND3):c.1536T>G (p.Asp512Glu)
NM_001378969.1(KCND3):c.1543A>C (p.Met515Leu)	rs369907159
NM_001378969.1(KCND3):c.1543A>G (p.Met515Val)
NM_001378969.1(KCND3):c.1561A>G (p.Met521Val)
NM_001378969.1(KCND3):c.1564G>A (p.Glu522Lys)
NM_001378969.1(KCND3):c.1615C>A (p.His539Asn)
NM_001378969.1(KCND3):c.1622G>A (p.Gly541Asp)
NM_001378969.1(KCND3):c.1660A>T (p.Thr554Ser)
NM_001378969.1(KCND3):c.166A>G (p.Thr56Ala)
NM_001378969.1(KCND3):c.1673C>G (p.Pro558Arg)
NM_001378969.1(KCND3):c.1677T>A (p.Asn559Lys)
NM_001378969.1(KCND3):c.1696C>T (p.Arg566Cys)
NM_001378969.1(KCND3):c.170C>T (p.Thr57Met)
NM_001378969.1(KCND3):c.1733T>C (p.Ile578Thr)
NM_001378969.1(KCND3):c.1736A>C (p.Gln579Pro)
NM_001378969.1(KCND3):c.1749G>C (p.Gln583His)
NM_001378969.1(KCND3):c.1756C>G (p.Leu586Val)	rs778053688
NM_001378969.1(KCND3):c.1762A>G (p.Thr588Ala)
NM_001378969.1(KCND3):c.178C>T (p.Arg60Cys)
NM_001378969.1(KCND3):c.1795G>A (p.Asp599Asn)
NM_001378969.1(KCND3):c.1873C>T (p.Pro625Ser)	rs2101452061
NM_001378969.1(KCND3):c.1888C>T (p.Arg630Trp)
NM_001378969.1(KCND3):c.1895C>G (p.Pro632Arg)
NM_001378969.1(KCND3):c.1897C>A (p.Pro633Thr)
NM_001378969.1(KCND3):c.1924A>T (p.Ile642Phe)	rs754759010
NM_001378969.1(KCND3):c.1942A>G (p.Asn648Asp)
NM_001378969.1(KCND3):c.239A>G (p.Lys80Arg)
NM_001378969.1(KCND3):c.295C>T (p.Arg99Cys)
NM_001378969.1(KCND3):c.367A>G (p.Ile123Val)
NM_001378969.1(KCND3):c.385G>A (p.Gly129Arg)
NM_001378969.1(KCND3):c.388G>A (p.Asp130Asn)
NM_001378969.1(KCND3):c.430G>C (p.Ala144Pro)
NM_001378969.1(KCND3):c.44C>T (p.Ala15Val)	rs866544148
NM_001378969.1(KCND3):c.460G>A (p.Glu154Lys)
NM_001378969.1(KCND3):c.491G>A (p.Ser164Asn)
NM_001378969.1(KCND3):c.497G>A (p.Arg166His)
NM_001378969.1(KCND3):c.506T>C (p.Met169Thr)
NM_001378969.1(KCND3):c.520G>A (p.Glu174Lys)
NM_001378969.1(KCND3):c.533C>T (p.Thr178Ile)
NM_001378969.1(KCND3):c.539C>T (p.Thr180Met)
NM_001378969.1(KCND3):c.59T>A (p.Met20Lys)
NM_001378969.1(KCND3):c.611C>T (p.Thr204Met)	rs2101997230
NM_001378969.1(KCND3):c.646C>A (p.Leu216Met)
NM_001378969.1(KCND3):c.647T>G (p.Leu216Arg)
NM_001378969.1(KCND3):c.878G>A (p.Arg293His)	rs1674965278
NM_001378969.1(KCND3):c.917G>A (p.Gly306Asp)	rs2101995501

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