ClinVar Miner

List of variants in gene FBXO11 reported as benign for not provided

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Gene type:
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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001190274.2(FBXO11):c.1578A>G (p.Ala526=) rs35935360 0.01480
NM_001190274.2(FBXO11):c.801+15T>A rs183571348 0.00131
NM_001190274.2(FBXO11):c.1154-19A>C rs186451058 0.00130
NM_001190274.2(FBXO11):c.232+7C>T rs752461788 0.00100
NM_001190274.2(FBXO11):c.717+17G>T rs182017112 0.00068
NM_001190274.2(FBXO11):c.443-20A>G rs199713192 0.00056
NM_001190274.2(FBXO11):c.587+16T>C rs200208204 0.00052
NM_001190274.2(FBXO11):c.1389T>C (p.Asp463=) rs199728471 0.00033
NM_001190274.2(FBXO11):c.361-5T>C rs186104745 0.00024
NM_001190274.2(FBXO11):c.1896A>G (p.Arg632=) rs185472550 0.00023
NM_001190274.2(FBXO11):c.587+15A>C rs766401172 0.00022
NM_001190274.2(FBXO11):c.1164A>G (p.Ala388=) rs529563653 0.00019
NM_001190274.2(FBXO11):c.1434G>A (p.Arg478=) rs200669207 0.00015
NM_001190274.2(FBXO11):c.1617-4A>G rs570549776 0.00015
NM_001190274.2(FBXO11):c.780T>C (p.Tyr260=) rs759824594 0.00014
NM_001190274.2(FBXO11):c.677A>G (p.Tyr226Cys) rs142422435 0.00013
NM_001190274.2(FBXO11):c.916A>G (p.Ile306Val) rs375970407 0.00011
NM_001190274.2(FBXO11):c.945A>G (p.Lys315=) rs139178411 0.00008
NM_001190274.2(FBXO11):c.2205C>T (p.Ile735=) rs201246111 0.00006
NM_001190274.2(FBXO11):c.609A>T (p.Val203=) rs773584366 0.00006
NM_001190274.2(FBXO11):c.360+5C>G rs756824715 0.00004
NM_001190274.2(FBXO11):c.1253A>G (p.His418Arg) rs889397926 0.00002
NM_001190274.2(FBXO11):c.2083+4T>G rs780793954 0.00001
NM_001190274.2(FBXO11):c.217A>G (p.Asn73Asp) rs1343785656 0.00001
NM_001190274.2(FBXO11):c.319T>C (p.Leu107=) rs772149952 0.00001
NM_001190274.2(FBXO11):c.335C>T (p.Ala112Val) rs142562364 0.00001
NM_001190274.2(FBXO11):c.882A>G (p.Ile294Met) rs948091027 0.00001
NM_001190274.2(FBXO11):c.937C>G (p.Pro313Ala) rs745529478 0.00001
NM_001190274.2(FBXO11):c.1041+16A>G rs191217715
NM_001190274.2(FBXO11):c.1153+16A>C rs201005367
NM_001190274.2(FBXO11):c.1398+13_1398+16del rs67864921
NM_001190274.2(FBXO11):c.1476G>A (p.Val492=)
NM_001190274.2(FBXO11):c.1616+10T>C
NM_001190274.2(FBXO11):c.1616+5T>C
NM_001190274.2(FBXO11):c.1617-18del
NM_001190274.2(FBXO11):c.1617-18dup rs535017411
NM_001190274.2(FBXO11):c.1701T>C (p.Tyr567=) rs753056273
NM_001190274.2(FBXO11):c.1702+4A>G
NM_001190274.2(FBXO11):c.1755G>A (p.Arg585=) rs555037249
NM_001190274.2(FBXO11):c.1920+6A>G
NM_001190274.2(FBXO11):c.1921-10del rs374445177
NM_001190274.2(FBXO11):c.200T>C (p.Leu67Pro)
NM_001190274.2(FBXO11):c.2084-4A>G rs750761143
NM_001190274.2(FBXO11):c.221_223del (p.Val74del) rs761010339
NM_001190274.2(FBXO11):c.267A>C (p.Glu89Asp)
NM_001190274.2(FBXO11):c.268T>C (p.Ser90Pro)
NM_001190274.2(FBXO11):c.376A>T (p.Thr126Ser) rs17036993
NM_001190274.2(FBXO11):c.427T>G (p.Ser143Ala) rs1284695050
NM_001190274.2(FBXO11):c.536C>G (p.Ala179Gly)
NM_001190274.2(FBXO11):c.583T>G (p.Leu195Val) rs2104855862
NM_001190274.2(FBXO11):c.659A>G (p.Gln220Arg)
NM_001190274.2(FBXO11):c.802-16A>G rs202141407
NM_001190274.2(FBXO11):c.802-17_802-16delinsAC
NM_001190274.2(FBXO11):c.924G>C (p.Met308Ile) rs1219431687
NM_001190274.2(FBXO11):c.935-7_935-5del rs1667499312

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