ClinVar Miner

List of variants reported as likely benign for Multiple endocrine neoplasia, type 4 by Invitae

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Total variants: 58
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HGVS dbSNP
NM_004064.4(CDKN1B):c.-29_-26delAGAG rs774454456
NM_004064.4(CDKN1B):c.114C>T (p.His38=) rs141178987
NM_004064.4(CDKN1B):c.126C>T (p.Thr42=) rs747582957
NM_004064.4(CDKN1B):c.12G>A (p.Val4=) rs1555085477
NM_004064.4(CDKN1B):c.153C>T (p.Asp51=) rs1455488274
NM_004064.4(CDKN1B):c.155T>G (p.Met52Arg) rs543122580
NM_004064.4(CDKN1B):c.168C>T (p.Ser56=) rs35456792
NM_004064.4(CDKN1B):c.177G>A (p.Lys59=) rs140927518
NM_004064.4(CDKN1B):c.201C>T (p.His67=) rs771682338
NM_004064.4(CDKN1B):c.207C>T (p.Pro69=) rs746849706
NM_004064.4(CDKN1B):c.208C>T (p.Leu70=) rs1565419399
NM_004064.4(CDKN1B):c.219G>A (p.Lys73=) rs573353679
NM_004064.4(CDKN1B):c.222C>T (p.Tyr74=) rs1592280959
NM_004064.4(CDKN1B):c.225G>C (p.Glu75Asp) rs139727620
NM_004064.4(CDKN1B):c.234G>A (p.Glu78=) rs751794433
NM_004064.4(CDKN1B):c.246C>T (p.Gly82=) rs376624980
NM_004064.4(CDKN1B):c.24C>T (p.Asn8=) rs371308246
NM_004064.4(CDKN1B):c.261C>T (p.Phe87=) rs368696530
NM_004064.4(CDKN1B):c.264C>T (p.Tyr88=) rs374493057
NM_004064.4(CDKN1B):c.267C>T (p.Tyr89=) rs532903617
NM_004064.4(CDKN1B):c.273C>T (p.Pro91=) rs761928140
NM_004064.4(CDKN1B):c.277C>T (p.Arg93Trp) rs140167393
NM_004064.4(CDKN1B):c.279G>A (p.Arg93=) rs766901538
NM_004064.4(CDKN1B):c.27G>A (p.Gly9=) rs1060503869
NM_004064.4(CDKN1B):c.282C>T (p.Pro94=) rs751288223
NM_004064.4(CDKN1B):c.283C>G (p.Pro95Ala) rs188579132
NM_004064.4(CDKN1B):c.285C>A (p.Pro95=) rs780148172
NM_004064.4(CDKN1B):c.294C>T (p.Ala98=) rs768919562
NM_004064.4(CDKN1B):c.309G>A (p.Ala103=) rs761029896
NM_004064.4(CDKN1B):c.326T>A (p.Val109Asp) rs2066827
NM_004064.4(CDKN1B):c.345G>A (p.Ala115=) rs199570763
NM_004064.4(CDKN1B):c.348G>A (p.Ala116=) rs1365789536
NM_004064.4(CDKN1B):c.356T>C (p.Ile119Thr) rs142833529
NM_004064.4(CDKN1B):c.366G>C (p.Pro122=) rs776945453
NM_004064.4(CDKN1B):c.373T>A (p.Ser125Thr) rs765681672
NM_004064.4(CDKN1B):c.384G>T (p.Thr128=) rs878854622
NM_004064.4(CDKN1B):c.387T>C (p.His129=) rs377573215
NM_004064.4(CDKN1B):c.396C>T (p.Asp132=) rs1592281203
NM_004064.4(CDKN1B):c.417C>T (p.Asp139=) rs747272462
NM_004064.4(CDKN1B):c.429G>A (p.Gly143=) rs764460528
NM_004064.4(CDKN1B):c.429G>T (p.Gly143=) rs764460528
NM_004064.4(CDKN1B):c.42G>A (p.Glu14=) rs747456770
NM_004064.4(CDKN1B):c.459G>A (p.Lys153=) rs766153167
NM_004064.4(CDKN1B):c.460C>A (p.Arg154=) rs1292160956
NM_004064.4(CDKN1B):c.471C>A (p.Thr157=) rs777875072
NM_004064.4(CDKN1B):c.476-10C>T rs200108977
NM_004064.4(CDKN1B):c.476-6_476-5delinsAT rs1555085703
NM_004064.4(CDKN1B):c.492C>T (p.Asn164=) rs762810555
NM_004064.4(CDKN1B):c.518A>G (p.Asn173Ser) rs141509450
NM_004064.4(CDKN1B):c.528C>T (p.Asp176=) rs779413893
NM_004064.4(CDKN1B):c.54C>T (p.Ala18=) rs151027466
NM_004064.4(CDKN1B):c.570G>A (p.Lys190=) rs1592281782
NM_004064.4(CDKN1B):c.576C>T (p.Gly192=) rs772023525
NM_004064.4(CDKN1B):c.579C>T (p.Leu193=) rs201701670
NM_004064.4(CDKN1B):c.588T>C (p.Arg196=) rs1592281803
NM_004064.4(CDKN1B):c.75G>A (p.Lys25=) rs367611328
NM_004064.4(CDKN1B):c.87C>T (p.Cys29=) rs767234696
NM_004064.4(CDKN1B):c.9C>T (p.Asn3=) rs1411622351

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