ClinVar Miner

List of variants in gene TRMU reported as likely benign for not provided

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Total variants: 34
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HGVS dbSNP
NM_018006.5(TRMU):c.-25G>A
NM_018006.5(TRMU):c.-26A>C
NM_018006.5(TRMU):c.1018+7G>C
NM_018006.5(TRMU):c.1018+9C>T rs373346869
NM_018006.5(TRMU):c.1035C>T (p.Thr345=)
NM_018006.5(TRMU):c.1053C>T (p.Thr351=) rs374614222
NM_018006.5(TRMU):c.1125C>T (p.Asp375=)
NM_018006.5(TRMU):c.1137C>T (p.Gly379=)
NM_018006.5(TRMU):c.1152G>A (p.Leu384=)
NM_018006.5(TRMU):c.1164G>A (p.Pro388=) rs202047181
NM_018006.5(TRMU):c.1188C>G (p.Gly396=) rs142346622
NM_018006.5(TRMU):c.1218C>T (p.Ser406=) rs754239335
NM_018006.5(TRMU):c.1227C>T (p.Asp409=)
NM_018006.5(TRMU):c.18C>T (p.His6=)
NM_018006.5(TRMU):c.248+9G>A
NM_018006.5(TRMU):c.248+9_248+18del rs763718617
NM_018006.5(TRMU):c.264G>A (p.Glu88=)
NM_018006.5(TRMU):c.296T>C (p.Ile99Thr) rs144054758
NM_018006.5(TRMU):c.30C>T (p.Ala10=)
NM_018006.5(TRMU):c.355+7A>G
NM_018006.5(TRMU):c.39C>G (p.Gly13=)
NM_018006.5(TRMU):c.479-10T>C rs202070165
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.633T>C (p.His211=)
NM_018006.5(TRMU):c.651+8T>C
NM_018006.5(TRMU):c.672C>T (p.Ile224=)
NM_018006.5(TRMU):c.753G>A (p.Lys251=)
NM_018006.5(TRMU):c.82+10C>T
NM_018006.5(TRMU):c.82+8G>A
NM_018006.5(TRMU):c.83-4G>A rs369925943
NM_018006.5(TRMU):c.83-5C>T
NM_018006.5(TRMU):c.834C>T (p.Tyr278=)
NM_018006.5(TRMU):c.9C>T (p.Ala3=)

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