ClinVar Miner

List of variants in gene CTU2 reported as benign for not provided

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Gene type:
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Total variants: 51
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HGVS dbSNP gnomAD frequency
NM_001012759.3(CTU2):c.1006-26A>G rs3826076 0.88981
NM_001012759.3(CTU2):c.1332T>C (p.Cys444=) rs8043637 0.87988
NM_001012759.3(CTU2):c.1201+29C>G rs8050715 0.87097
NM_001012759.3(CTU2):c.344-67G>A rs7205989 0.51964
NM_001012759.3(CTU2):c.757A>G (p.Met253Val) rs11549837 0.39293
NM_001012759.3(CTU2):c.1247A>G (p.Gln416Arg) rs8059048 0.22042
NM_001012759.3(CTU2):c.737+10C>T rs12148926 0.17143
NM_001012759.3(CTU2):c.909G>A (p.Val303=) rs2290904 0.15086
NM_001012759.3(CTU2):c.556C>T (p.His186Tyr) rs2290895 0.13873
NM_001012759.3(CTU2):c.873+10G>A rs4782320 0.09800
NM_001012759.3(CTU2):c.1280G>A (p.Arg427Gln) rs11549835 0.09541
NM_001012759.3(CTU2):c.1065C>G (p.Thr355=) rs73262673 0.04325
NM_001012759.3(CTU2):c.322G>C (p.Ala108Pro) rs61738915 0.01749
NM_001012759.3(CTU2):c.969C>T (p.Ser323=) rs2340974 0.01577
NM_001012759.3(CTU2):c.25G>A (p.Gly9Arg) rs137933845 0.01519
NM_001012759.3(CTU2):c.282+18C>T rs147078272 0.01418
NM_001012759.3(CTU2):c.1347C>T (p.Cys449=) rs2340976 0.01031
NM_001012759.3(CTU2):c.1289C>T (p.Pro430Leu) rs61744519 0.00808
NM_001012759.3(CTU2):c.501G>A (p.Leu167=) rs138003612 0.00798
NM_001012759.3(CTU2):c.522C>T (p.Tyr174=) rs76614176 0.00545
NM_001012759.3(CTU2):c.1269G>A (p.Leu423=) rs28672793 0.00540
NM_001012759.3(CTU2):c.1221G>A (p.Gly407=) rs141242265 0.00521
NM_001012759.3(CTU2):c.1357G>A (p.Asp453Asn) rs140495759 0.00440
NM_001012759.3(CTU2):c.69-19C>T rs185353598 0.00369
NM_001012759.3(CTU2):c.1425A>G (p.Ser475=) rs78212226 0.00249
NM_001012759.3(CTU2):c.616C>G (p.Pro206Ala) rs140091320 0.00230
NM_001012759.3(CTU2):c.1531G>A (p.Glu511Lys) rs201215099 0.00226
NM_001012759.3(CTU2):c.1097+14_1097+23del rs1555551063
NM_001012759.3(CTU2):c.1097+1GT[4] rs149847195
NM_001012759.3(CTU2):c.1097+6_1097+11del
NM_001012759.3(CTU2):c.1097+6_1097+32del
NM_001012759.3(CTU2):c.1120G>T (p.Gly374Cys) rs61730418
NM_001012759.3(CTU2):c.1127G>A (p.Arg376Gln) rs61730419
NM_001012759.3(CTU2):c.1153G>A (p.Gly385Ser)
NM_001012759.3(CTU2):c.1191C>T (p.Val397=)
NM_001012759.3(CTU2):c.1399C>T (p.Arg467Cys) rs139862860
NM_001012759.3(CTU2):c.1478+7G>A
NM_001012759.3(CTU2):c.353C>T (p.Ala118Val) rs61744025
NM_001012759.3(CTU2):c.456G>C (p.Val152=) rs2290896
NM_001012759.3(CTU2):c.528G>C (p.Ala176=)
NM_001012759.3(CTU2):c.570C>T (p.Ala190=)
NM_001012759.3(CTU2):c.68+20C>G
NM_001012759.3(CTU2):c.69-16C>A rs11641194
NM_001012759.3(CTU2):c.737+10_737+52del rs777538410
NM_001012759.3(CTU2):c.737+20_737+21insTTCCCCGGGCCCTGACCCCCACTCATGCCCCTGAGAGCCCC rs1567649917
NM_001012759.3(CTU2):c.737+21_737+63del rs776264293
NM_001012759.3(CTU2):c.737+21del rs67815044
NM_001012759.3(CTU2):c.737+64_737+105del rs750411872
NM_001012759.3(CTU2):c.74A>C (p.Glu25Ala)
NM_001012759.3(CTU2):c.771C>T (p.His257=) rs73262667
NM_001012759.3(CTU2):c.994G>A (p.Val332Ile) rs4782321

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