ClinVar Miner

List of variants in gene NETO2 reported as uncertain significance

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Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_018092.5(NETO2):c.613G>A (p.Val205Ile) rs139362451 0.00044
NM_018092.5(NETO2):c.1496G>A (p.Arg499Gln) rs766715523 0.00013
NM_018092.5(NETO2):c.746A>G (p.Glu249Gly) rs766042295 0.00011
NM_018092.5(NETO2):c.1147G>A (p.Ala383Thr) rs144722995 0.00009
NM_018092.5(NETO2):c.1157A>G (p.Lys386Arg) rs149384006 0.00007
NM_018092.5(NETO2):c.1250A>G (p.Glu417Gly) rs377005431 0.00005
NM_018092.5(NETO2):c.1337G>A (p.Ser446Asn) rs201675106 0.00003
NM_018092.5(NETO2):c.695A>G (p.Asn232Ser) rs1306505675 0.00003
NM_018092.5(NETO2):c.842G>A (p.Arg281Gln) rs1384956543 0.00003
NM_018092.5(NETO2):c.1053T>G (p.Ile351Met) rs750674844 0.00001
NM_018092.5(NETO2):c.1202T>C (p.Phe401Ser) rs1963118833 0.00001
NM_018092.5(NETO2):c.1349G>A (p.Ser450Asn) rs750129372 0.00001
NM_018092.5(NETO2):c.274T>C (p.Tyr92His) rs746342583 0.00001
NM_018092.5(NETO2):c.286C>A (p.Pro96Thr) rs751767431 0.00001
NM_018092.5(NETO2):c.355G>A (p.Asp119Asn) rs771729249 0.00001
NM_018092.5(NETO2):c.389T>G (p.Ile130Ser) rs1964198713 0.00001
NM_018092.5(NETO2):c.694A>G (p.Asn232Asp) rs1334094714 0.00001
NM_018092.5(NETO2):c.857G>A (p.Arg286Gln) rs570205519 0.00001
NM_018092.5(NETO2):c.1103T>C (p.Val368Ala) rs2549028048
NM_018092.5(NETO2):c.1135G>A (p.Ala379Thr) rs764980937
NM_018092.5(NETO2):c.1169A>G (p.Gln390Arg)
NM_018092.5(NETO2):c.1245G>T (p.Leu415Phe)
NM_018092.5(NETO2):c.1279C>T (p.Arg427Cys) rs773680548
NM_018092.5(NETO2):c.1316A>G (p.His439Arg) rs2549027597
NM_018092.5(NETO2):c.1325C>T (p.Ser442Leu)
NM_018092.5(NETO2):c.1376T>G (p.Leu459Arg)
NM_018092.5(NETO2):c.1492G>A (p.Asp498Asn)
NM_018092.5(NETO2):c.149G>T (p.Arg50Leu)
NM_018092.5(NETO2):c.1503G>A (p.Met501Ile) rs2549027149
NM_018092.5(NETO2):c.1532G>C (p.Arg511Thr) rs193920943
NM_018092.5(NETO2):c.205A>G (p.Asn69Asp)
NM_018092.5(NETO2):c.282A>G (p.Ile94Met)
NM_018092.5(NETO2):c.325G>A (p.Asp109Asn)
NM_018092.5(NETO2):c.419A>G (p.Lys140Arg)
NM_018092.5(NETO2):c.515A>G (p.Asn172Ser)
NM_018092.5(NETO2):c.538G>A (p.Glu180Lys)
NM_018092.5(NETO2):c.583C>G (p.Gln195Glu)
NM_018092.5(NETO2):c.608A>G (p.Gln203Arg)
NM_018092.5(NETO2):c.631A>G (p.Ile211Val)
NM_018092.5(NETO2):c.647A>T (p.Lys216Ile) rs2549055426
NM_018092.5(NETO2):c.860T>C (p.Met287Thr) rs1963744390
NM_018092.5(NETO2):c.877G>T (p.Val293Leu)
NM_018092.5(NETO2):c.914A>T (p.His305Leu) rs769338360
NM_018092.5(NETO2):c.985A>T (p.Asn329Tyr) rs756769234

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