ClinVar Miner

List of variants in gene MMUT reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 17
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NM_000255.4(MMUT):c.-16G>A rs781555363
NM_000255.4(MMUT):c.1041A>G (p.Leu347=) rs1454849970
NM_000255.4(MMUT):c.1083+20T>C rs200148994
NM_000255.4(MMUT):c.1206T>G (p.Ala402=) rs142539215
NM_000255.4(MMUT):c.1333-18T>G rs111667453
NM_000255.4(MMUT):c.1410A>G (p.Glu470=) rs755553945
NM_000255.4(MMUT):c.1515T>C (p.Ile505=) rs772936850
NM_000255.4(MMUT):c.1676+10T>C rs199886805
NM_000255.4(MMUT):c.1808+15T>C rs369131814
NM_000255.4(MMUT):c.189C>A (p.Thr63=) rs777167901
NM_000255.4(MMUT):c.1944C>A (p.Gly648=) rs758674900
NM_000255.4(MMUT):c.1956+16G>T rs1057521406
NM_000255.4(MMUT):c.2022C>T (p.Leu674=) rs772652266
NM_000255.4(MMUT):c.363G>A (p.Lys121=) rs772753347
NM_000255.4(MMUT):c.393G>A (p.Gln131=) rs145682249
NM_000255.4(MMUT):c.423G>A (p.Ala141=) rs547142339
NM_000255.4(MMUT):c.461G>A (p.Arg154His) rs142068898

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