ClinVar Miner

List of variants in gene TRMU reported as likely benign

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Gene type:
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Total variants: 47
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HGVS dbSNP
NM_018006.4(TRMU):c.-117G>C rs116519615
NM_018006.4(TRMU):c.-128A>G rs141601555
NM_018006.4(TRMU):c.-178G>A rs114587018
NM_018006.5(TRMU):c.*124G>C rs116303153
NM_018006.5(TRMU):c.*151C>T rs116347546
NM_018006.5(TRMU):c.*210G>C rs141551983
NM_018006.5(TRMU):c.*266_*267AG[1] rs149055127
NM_018006.5(TRMU):c.-15T>C rs764076380
NM_018006.5(TRMU):c.-19G>C rs886057609
NM_018006.5(TRMU):c.-25G>A
NM_018006.5(TRMU):c.-26A>C
NM_018006.5(TRMU):c.-36C>G rs560661382
NM_018006.5(TRMU):c.-44G>A rs370964036
NM_018006.5(TRMU):c.1007A>C (p.Gln336Pro) rs796052192
NM_018006.5(TRMU):c.1018+9C>T rs373346869
NM_018006.5(TRMU):c.1053C>T (p.Thr351=) rs374614222
NM_018006.5(TRMU):c.1062G>A (p.Val354=) rs368415197
NM_018006.5(TRMU):c.1093A>C (p.Thr365Pro) rs138586787
NM_018006.5(TRMU):c.10T>G (p.Leu4Val) rs114302881
NM_018006.5(TRMU):c.1125C>A (p.Asp375Glu) rs779022860
NM_018006.5(TRMU):c.1158G>A (p.Leu386=) rs79874854
NM_018006.5(TRMU):c.1164G>A (p.Pro388=) rs202047181
NM_018006.5(TRMU):c.1192C>T (p.Arg398Cys) rs34152016
NM_018006.5(TRMU):c.1193G>A (p.Arg398His) rs139351059
NM_018006.5(TRMU):c.1218C>T (p.Ser406=) rs754239335
NM_018006.5(TRMU):c.1246G>T (p.Gly416Cys) rs150043707
NM_018006.5(TRMU):c.248+19A>C rs1057521579
NM_018006.5(TRMU):c.429C>T (p.His143=) rs746421213
NM_018006.5(TRMU):c.430G>A (p.Val144Ile) rs367570778
NM_018006.5(TRMU):c.442G>A (p.Glu148Lys) rs34012206
NM_018006.5(TRMU):c.469G>A (p.Val157Ile) rs201755743
NM_018006.5(TRMU):c.479-10T>C rs202070165
NM_018006.5(TRMU):c.479C>T (p.Ala160Val) rs35338668
NM_018006.5(TRMU):c.552C>T (p.Ala184=) rs35772382
NM_018006.5(TRMU):c.567C>G (p.Ile189Met) rs192537315
NM_018006.5(TRMU):c.576G>C (p.Leu192=) rs1319509730
NM_018006.5(TRMU):c.60C>A (p.Ala20=) rs1188059840
NM_018006.5(TRMU):c.75G>T (p.Arg25Ser) rs2272938
NM_018006.5(TRMU):c.768T>C (p.His256=) rs1555899299
NM_018006.5(TRMU):c.772+11G>C rs1262602634
NM_018006.5(TRMU):c.83-11C>A rs1057523042
NM_018006.5(TRMU):c.864C>T (p.Asp288=) rs61737827
NM_018006.5(TRMU):c.873+12G>A rs540183174
NM_018006.5(TRMU):c.900G>T (p.Leu300=) rs113846383
NM_018006.5(TRMU):c.927C>T (p.Arg309=) rs9627420
NM_018006.5(TRMU):c.942G>A (p.Ala314=) rs767891094
NM_018006.5(TRMU):c.9C>G (p.Ala3=) rs75417986

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