ClinVar Miner

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

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Gene type:
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Total variants: 23
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HGVS dbSNP
NM_000255.4(MMUT):c.1079A>G (p.Glu360Gly) rs1442661766
NM_000255.4(MMUT):c.1115T>C (p.Ile372Thr) rs150968643
NM_000255.4(MMUT):c.1125G>A (p.Met375Ile) rs148091558
NM_000255.4(MMUT):c.1332+3A>C rs367641890
NM_000255.4(MMUT):c.1357G>A (p.Gly453Ser) rs1022821298
NM_000255.4(MMUT):c.1360G>A (p.Gly454Arg) rs794727842
NM_000255.4(MMUT):c.1417G>T (p.Ala473Ser) rs188766510
NM_000255.4(MMUT):c.1837C>A (p.Arg613Ser)
NM_000255.4(MMUT):c.1849_1851CTT[1] (p.Leu618del) rs398123277
NM_000255.4(MMUT):c.1936del (p.Asp646fs) rs1561952070
NM_000255.4(MMUT):c.205A>G (p.Ile69Val) rs115923556
NM_000255.4(MMUT):c.317C>T (p.Thr106Ile) rs1561959708
NM_000255.4(MMUT):c.385+14G>A rs199992904
NM_000255.4(MMUT):c.393G>A (p.Gln131=) rs145682249
NM_000255.4(MMUT):c.431G>A (p.Arg144His) rs776621768
NM_000255.4(MMUT):c.446A>T (p.Asp149Val) rs1194327802
NM_000255.4(MMUT):c.743A>G (p.Tyr248Cys) rs757594175
NM_000255.4(MMUT):c.753G>C (p.Lys251Asn) rs727504021
NM_000255.4(MMUT):c.754C>T (p.His252Tyr) rs796052010
NM_000255.4(MMUT):c.781A>G (p.Ile261Val) rs375054307
NM_000255.4(MMUT):c.833C>T (p.Ala278Val) rs1561958387
NM_000255.4(MMUT):c.878A>G (p.Gln293Arg) rs138374956
NM_000255.4(MMUT):c.912-1G>A rs1561957527

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