ClinVar Miner

List of variants in gene MVK reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
Download table as spreadsheet
NM_000431.4(MVK):c.1139A>G (p.His380Arg) rs104895324
NM_000431.4(MVK):c.119G>A (p.Arg40Gln) rs373095009
NM_000431.4(MVK):c.14T>C (p.Val5Ala) rs141765653
NM_000431.4(MVK):c.151C>T (p.Leu51Phe) rs892779197
NM_000431.4(MVK):c.155G>T (p.Ser52Ile)
NM_000431.4(MVK):c.227-18T>C rs876661049
NM_000431.4(MVK):c.238G>A (p.Val80Ile) rs76914224
NM_000431.4(MVK):c.287G>T (p.Gly96Val) rs1337856151
NM_000431.4(MVK):c.298G>A (p.Asp100Asn)
NM_000431.4(MVK):c.29C>T (p.Ala10Val)
NM_000431.4(MVK):c.32C>T (p.Pro11Leu) rs876661001
NM_000431.4(MVK):c.441C>T (p.Ala147=) rs138342076
NM_000431.4(MVK):c.498C>A (p.Asn166Lys) rs765975337
NM_000431.4(MVK):c.518G>A (p.Cys173Tyr) rs1267793765
NM_000431.4(MVK):c.614A>G (p.Asn205Ser) rs767853272
NM_000431.4(MVK):c.719C>G (p.Pro240Arg) rs1458254066
NM_000431.4(MVK):c.785C>T (p.Ala262Val) rs763106439
NM_000431.4(MVK):c.787C>T (p.Pro263Ser)
NM_000431.4(MVK):c.819G>A (p.Leu273=) rs876661134
NM_000431.4(MVK):c.832G>A (p.Val278Met) rs574045811
NM_000431.4(MVK):c.874C>T (p.Leu292Phe) rs145586352
NM_000431.4(MVK):c.924C>T (p.Leu308=) rs72648042
NM_000431.4(MVK):c.936C>T (p.His312=) rs1212639017

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.