ClinVar Miner

List of variants in gene RANBP2 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 198
Download table as spreadsheet
HGVS dbSNP
NM_006267.5(RANBP2):c.1063+8dup
NM_006267.5(RANBP2):c.1065G>A (p.Gly355=)
NM_006267.5(RANBP2):c.1149T>C (p.Ser383=)
NM_006267.5(RANBP2):c.1225A>G (p.Ile409Val) rs201087513
NM_006267.5(RANBP2):c.1273+9T>C
NM_006267.5(RANBP2):c.1274-13A>T
NM_006267.5(RANBP2):c.1284A>G (p.Arg428=) rs142514679
NM_006267.5(RANBP2):c.1361G>A (p.Arg454Gln) rs779203901
NM_006267.5(RANBP2):c.1398T>C (p.His466=)
NM_006267.5(RANBP2):c.140+9A>T
NM_006267.5(RANBP2):c.156C>T (p.Tyr52=)
NM_006267.5(RANBP2):c.1737A>C (p.Ala579=)
NM_006267.5(RANBP2):c.1738G>A (p.Glu580Lys) rs1057956
NM_006267.5(RANBP2):c.1756-10T>C
NM_006267.5(RANBP2):c.1761C>T (p.Ser587=)
NM_006267.5(RANBP2):c.1770T>C (p.Asn590=) rs1573774225
NM_006267.5(RANBP2):c.1776T>C (p.Phe592=) rs755487849
NM_006267.5(RANBP2):c.1803A>G (p.Arg601=)
NM_006267.5(RANBP2):c.1833A>G (p.Pro611=)
NM_006267.5(RANBP2):c.1917+9G>A
NM_006267.5(RANBP2):c.1918-11TG[2]
NM_006267.5(RANBP2):c.1959T>C (p.Thr653=)
NM_006267.5(RANBP2):c.2040T>C (p.Tyr680=)
NM_006267.5(RANBP2):c.2056-10A>G rs539183099
NM_006267.5(RANBP2):c.2056-19A>G rs199880095
NM_006267.5(RANBP2):c.2056-4A>T rs372329184
NM_006267.5(RANBP2):c.2084A>C (p.Glu695Ala) rs148298842
NM_006267.5(RANBP2):c.2103T>C (p.Pro701=)
NM_006267.5(RANBP2):c.2142C>T (p.Thr714=) rs371899344
NM_006267.5(RANBP2):c.2148C>T (p.Asp716=) rs1573777630
NM_006267.5(RANBP2):c.2157A>T (p.Ile719=)
NM_006267.5(RANBP2):c.2196C>T (p.Val732=)
NM_006267.5(RANBP2):c.2203-8A>G rs372713342
NM_006267.5(RANBP2):c.2230G>C (p.Glu744Gln) rs2912840
NM_006267.5(RANBP2):c.2243C>T (p.Ser748Leu) rs200940828
NM_006267.5(RANBP2):c.2244A>G (p.Ser748=) rs1488046156
NM_006267.5(RANBP2):c.225C>T (p.Asn75=)
NM_006267.5(RANBP2):c.2268T>C (p.Tyr756=) rs1573780904
NM_006267.5(RANBP2):c.2302T>C (p.Leu768=)
NM_006267.5(RANBP2):c.2313A>G (p.Ala771=)
NM_006267.5(RANBP2):c.2337A>C (p.Thr779=)
NM_006267.5(RANBP2):c.2340G>A (p.Pro780=) rs2912839
NM_006267.5(RANBP2):c.2343T>C (p.Ser781=)
NM_006267.5(RANBP2):c.2379C>T (p.Tyr793=) rs1558908350
NM_006267.5(RANBP2):c.2448A>G (p.Gln816=)
NM_006267.5(RANBP2):c.2508A>G (p.Ala836=)
NM_006267.5(RANBP2):c.2511C>A (p.Ser837=)
NM_006267.5(RANBP2):c.2637G>A (p.Gln879=)
NM_006267.5(RANBP2):c.2698-4T>C
NM_006267.5(RANBP2):c.2700C>T (p.Gly900=)
NM_006267.5(RANBP2):c.2766C>T (p.His922=)
NM_006267.5(RANBP2):c.2829A>G (p.Ala943=)
NM_006267.5(RANBP2):c.2862A>G (p.Leu954=) rs374697321
NM_006267.5(RANBP2):c.288T>G (p.Leu96=) rs755002297
NM_006267.5(RANBP2):c.2895T>C (p.Asn965=)
NM_006267.5(RANBP2):c.2943C>T (p.Phe981=) rs1186427284
NM_006267.5(RANBP2):c.294G>A (p.Leu98=)
NM_006267.5(RANBP2):c.2954C>T (p.Pro985Leu)
NM_006267.5(RANBP2):c.3060A>G (p.Pro1020=) rs1312609974
NM_006267.5(RANBP2):c.3153T>C (p.Val1051=) rs372530448
NM_006267.5(RANBP2):c.3226T>G (p.Leu1076Val) rs142768885
NM_006267.5(RANBP2):c.324T>C (p.Asp108=) rs375199174
NM_006267.5(RANBP2):c.3350C>T (p.Ser1117Leu) rs137976808
NM_006267.5(RANBP2):c.3351G>A (p.Ser1117=) rs746610775
NM_006267.5(RANBP2):c.3363G>T (p.Lys1121Asn) rs112835359
NM_006267.5(RANBP2):c.3376C>T (p.Arg1126Trp) rs370285906
NM_006267.5(RANBP2):c.3387T>C (p.Asp1129=)
NM_006267.5(RANBP2):c.3399T>G (p.Thr1133=)
NM_006267.5(RANBP2):c.342A>T (p.Ala114=) rs140650569
NM_006267.5(RANBP2):c.3537T>C (p.Pro1179=)
NM_006267.5(RANBP2):c.3585T>C (p.Phe1195=)
NM_006267.5(RANBP2):c.3630A>G (p.Glu1210=)
NM_006267.5(RANBP2):c.366C>A (p.Ala122=)
NM_006267.5(RANBP2):c.3945G>A (p.Ala1315=)
NM_006267.5(RANBP2):c.4026G>T (p.Leu1342=)
NM_006267.5(RANBP2):c.4047A>G (p.Ala1349=)
NM_006267.5(RANBP2):c.4053A>G (p.Lys1351=)
NM_006267.5(RANBP2):c.4080C>T (p.Ser1360=)
NM_006267.5(RANBP2):c.4152G>A (p.Glu1384=)
NM_006267.5(RANBP2):c.4161C>T (p.Gly1387=) rs1474575032
NM_006267.5(RANBP2):c.4207A>G (p.Asn1403Asp) rs773879572
NM_006267.5(RANBP2):c.4331C>T (p.Ala1444Val)
NM_006267.5(RANBP2):c.4350A>G (p.Ser1450=)
NM_006267.5(RANBP2):c.4386A>G (p.Gly1462=)
NM_006267.5(RANBP2):c.4404T>C (p.Ile1468=)
NM_006267.5(RANBP2):c.4482G>A (p.Gly1494=)
NM_006267.5(RANBP2):c.4498G>C (p.Ala1500Pro) rs145284139
NM_006267.5(RANBP2):c.4515G>A (p.Pro1505=)
NM_006267.5(RANBP2):c.4534G>T (p.Ala1512Ser) rs184236392
NM_006267.5(RANBP2):c.4542T>C (p.Ser1514=)
NM_006267.5(RANBP2):c.468A>G (p.Ser156=) rs1573715364
NM_006267.5(RANBP2):c.4707G>A (p.Pro1569=) rs757396599
NM_006267.5(RANBP2):c.4752T>C (p.Phe1584=) rs1553495996
NM_006267.5(RANBP2):c.4791C>T (p.Ser1597=) rs547882747
NM_006267.5(RANBP2):c.492C>T (p.Asp164=)
NM_006267.5(RANBP2):c.4950A>G (p.Thr1650=) rs1553496153
NM_006267.5(RANBP2):c.4998G>A (p.Glu1666=)
NM_006267.5(RANBP2):c.5034T>C (p.Asn1678=)
NM_006267.5(RANBP2):c.5040C>T (p.Ala1680=) rs552993785
NM_006267.5(RANBP2):c.5166T>G (p.Thr1722=)
NM_006267.5(RANBP2):c.5175A>G (p.Glu1725=) rs535428027
NM_006267.5(RANBP2):c.541T>C (p.Leu181=)
NM_006267.5(RANBP2):c.543G>A (p.Leu181=) rs146460580
NM_006267.5(RANBP2):c.5561A>G (p.Asn1854Ser) rs141379413
NM_006267.5(RANBP2):c.5613A>T (p.Ser1871=)
NM_006267.5(RANBP2):c.561C>T (p.His187=) rs761758022
NM_006267.5(RANBP2):c.5801G>A (p.Arg1934His)
NM_006267.5(RANBP2):c.5825G>T (p.Ser1942Ile) rs201476147
NM_006267.5(RANBP2):c.5871A>G (p.Glu1957=) rs202117246
NM_006267.5(RANBP2):c.5950G>A (p.Gly1984Ser) rs375852855
NM_006267.5(RANBP2):c.5979C>T (p.Ser1993=) rs757493880
NM_006267.5(RANBP2):c.6024C>T (p.Ser2008=)
NM_006267.5(RANBP2):c.6033C>T (p.Ile2011=) rs1360566375
NM_006267.5(RANBP2):c.6039T>C (p.Phe2013=)
NM_006267.5(RANBP2):c.6060C>T (p.Pro2020=) rs4012040
NM_006267.5(RANBP2):c.606A>G (p.Glu202=)
NM_006267.5(RANBP2):c.6098A>G (p.Lys2033Arg) rs146851340
NM_006267.5(RANBP2):c.6120A>G (p.Val2040=) rs1056562628
NM_006267.5(RANBP2):c.6163A>C (p.Arg2055=)
NM_006267.5(RANBP2):c.6171G>A (p.Leu2057=) rs199917317
NM_006267.5(RANBP2):c.6276G>A (p.Thr2092=)
NM_006267.5(RANBP2):c.627G>A (p.Gln209=) rs1453197920
NM_006267.5(RANBP2):c.6282C>T (p.Asn2094=)
NM_006267.5(RANBP2):c.6291T>C (p.Pro2097=)
NM_006267.5(RANBP2):c.630C>T (p.Thr210=)
NM_006267.5(RANBP2):c.6312A>G (p.Ala2104=) rs751303610
NM_006267.5(RANBP2):c.6342T>C (p.Asp2114=) rs529005450
NM_006267.5(RANBP2):c.636+16T>C
NM_006267.5(RANBP2):c.6391C>T (p.Leu2131=)
NM_006267.5(RANBP2):c.6393G>A (p.Leu2131=)
NM_006267.5(RANBP2):c.6461C>G (p.Pro2154Arg) rs751375908
NM_006267.5(RANBP2):c.6613G>C (p.Gly2205Arg) rs755789696
NM_006267.5(RANBP2):c.6680A>G (p.Tyr2227Cys) rs2557901
NM_006267.5(RANBP2):c.6792A>C (p.Thr2264=) rs773147227
NM_006267.5(RANBP2):c.6955C>T (p.Leu2319=)
NM_006267.5(RANBP2):c.7026T>C (p.Tyr2342=)
NM_006267.5(RANBP2):c.7039G>C (p.Gly2347Arg) rs151064332
NM_006267.5(RANBP2):c.7182T>C (p.Asn2394=)
NM_006267.5(RANBP2):c.7293G>T (p.Ser2431=) rs774092353
NM_006267.5(RANBP2):c.732T>G (p.Leu244=)
NM_006267.5(RANBP2):c.7332A>G (p.Glu2444=)
NM_006267.5(RANBP2):c.7340C>T (p.Ser2447Phe) rs200750445
NM_006267.5(RANBP2):c.7411G>A (p.Val2471Ile)
NM_006267.5(RANBP2):c.7463T>C (p.Val2488Ala) rs189289937
NM_006267.5(RANBP2):c.7464A>G (p.Val2488=) rs368598843
NM_006267.5(RANBP2):c.7474A>G (p.Thr2492Ala) rs2693103
NM_006267.5(RANBP2):c.7596A>G (p.Pro2532=)
NM_006267.5(RANBP2):c.7602A>G (p.Ala2534=) rs759564858
NM_006267.5(RANBP2):c.7605C>T (p.Phe2535=)
NM_006267.5(RANBP2):c.7674T>C (p.Ser2558=)
NM_006267.5(RANBP2):c.7751A>G (p.Asp2584Gly) rs138022657
NM_006267.5(RANBP2):c.7827C>T (p.Tyr2609=) rs371875659
NM_006267.5(RANBP2):c.783-7A>G
NM_006267.5(RANBP2):c.7923C>T (p.Thr2641=)
NM_006267.5(RANBP2):c.7966A>G (p.Thr2656Ala) rs148596328
NM_006267.5(RANBP2):c.7995T>C (p.Asp2665=)
NM_006267.5(RANBP2):c.8020+10_8020+11del
NM_006267.5(RANBP2):c.8020+7C>T rs1573831757
NM_006267.5(RANBP2):c.8021-7T>C rs1573833135
NM_006267.5(RANBP2):c.8031C>T (p.Phe2677=)
NM_006267.5(RANBP2):c.8075G>A (p.Gly2692Asp) rs111958052
NM_006267.5(RANBP2):c.8100A>G (p.Glu2700=)
NM_006267.5(RANBP2):c.8106T>C (p.Asn2702=)
NM_006267.5(RANBP2):c.8125G>A (p.Glu2709Lys) rs373969193
NM_006267.5(RANBP2):c.8166G>A (p.Glu2722=) rs895968968
NM_006267.5(RANBP2):c.8262A>G (p.Gln2754=) rs749840401
NM_006267.5(RANBP2):c.8292+8C>A
NM_006267.5(RANBP2):c.8293-6_8293-5del
NM_006267.5(RANBP2):c.8334A>G (p.Val2778=) rs758018669
NM_006267.5(RANBP2):c.8346G>A (p.Gly2782=)
NM_006267.5(RANBP2):c.8385A>G (p.Glu2795=) rs774055387
NM_006267.5(RANBP2):c.8415A>G (p.Ser2805=) rs751209914
NM_006267.5(RANBP2):c.8461A>C (p.Thr2821Pro) rs142231499
NM_006267.5(RANBP2):c.8497+8_8497+10del rs1573843165
NM_006267.5(RANBP2):c.8498-5G>A
NM_006267.5(RANBP2):c.8589T>C (p.Phe2863=) rs1573846232
NM_006267.5(RANBP2):c.8613A>G (p.Gln2871=)
NM_006267.5(RANBP2):c.8670C>T (p.Ala2890=) rs199918785
NM_006267.5(RANBP2):c.8700T>C (p.Ser2900=) rs750711827
NM_006267.5(RANBP2):c.8761-4A>G rs199908301
NM_006267.5(RANBP2):c.8761-7A>G
NM_006267.5(RANBP2):c.8859C>T (p.Arg2953=) rs779450120
NM_006267.5(RANBP2):c.8916A>C (p.Leu2972=) rs1553502610
NM_006267.5(RANBP2):c.9067A>C (p.Arg3023=)
NM_006267.5(RANBP2):c.9228T>G (p.Pro3076=)
NM_006267.5(RANBP2):c.9243T>C (p.Thr3081=) rs752209534
NM_006267.5(RANBP2):c.9258A>C (p.Ser3086=)
NM_006267.5(RANBP2):c.9346G>A (p.Val3116Ile)
NM_006267.5(RANBP2):c.9354A>G (p.Pro3118=) rs201982385
NM_006267.5(RANBP2):c.9369+4G>A rs139387463
NM_006267.5(RANBP2):c.9369+8T>C rs534483974
NM_006267.5(RANBP2):c.9405A>G (p.Gly3135=) rs1553503136
NM_006267.5(RANBP2):c.9408G>A (p.Gln3136=) rs1429024597
NM_006267.5(RANBP2):c.9435T>C (p.Asp3145=)
NM_006267.5(RANBP2):c.9504T>C (p.Asn3168=)
NM_006267.5(RANBP2):c.951A>C (p.Ala317=)
NM_006267.5(RANBP2):c.951A>G (p.Ala317=) rs750467478
NM_006267.5(RANBP2):c.951A>T (p.Ala317=)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.