ClinVar Miner

List of variants in gene NDUFA10 reported as likely benign for not specified

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_004544.4(NDUFA10):c.105A>G (p.Lys35=) rs2083411 0.70392
NM_004544.4(NDUFA10):c.771A>G (p.Gln257=) rs13848 0.38961
NM_004544.4(NDUFA10):c.749+16G>A rs375221991 0.00095
NM_004544.4(NDUFA10):c.1000-5C>G rs201255198 0.00048
NM_004544.4(NDUFA10):c.312C>T (p.Leu104=) rs145407882 0.00014
NM_004544.4(NDUFA10):c.548-15T>C rs367815275 0.00013
NM_004544.4(NDUFA10):c.-37C>G rs532866878 0.00010
NM_004544.4(NDUFA10):c.749+15C>T rs369729748 0.00009
NM_004544.4(NDUFA10):c.1005G>A (p.Pro335=) rs778173280 0.00006
NM_004544.4(NDUFA10):c.461-12A>G rs372439113 0.00006
NM_004544.4(NDUFA10):c.71G>T (p.Arg24Leu) rs863224083 0.00006
NM_004544.4(NDUFA10):c.549T>C (p.Cys183=) rs149783296 0.00004
NM_004544.4(NDUFA10):c.*3G>A rs758335453 0.00003
NM_004544.4(NDUFA10):c.297A>G (p.Gly99=) rs1057523358 0.00003
NM_004544.4(NDUFA10):c.264A>G (p.Glu88=) rs776242214 0.00001
NM_004544.4(NDUFA10):c.516G>A (p.Ala172=) rs762553028 0.00001
NM_004544.4(NDUFA10):c.547+18A>G rs748355238 0.00001
NM_004544.4(NDUFA10):c.870T>C (p.Thr290=) rs765127812 0.00001
NM_004544.4(NDUFA10):c.*8G>T rs370647399
NM_004544.4(NDUFA10):c.1032C>T (p.Asn344=) rs1019794328
NM_004544.4(NDUFA10):c.215A>G (p.Lys72Arg) rs863224080
NM_004544.4(NDUFA10):c.804+12G>C rs1318677453

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