ClinVar Miner

List of variants in gene MAN2B1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 282
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HGVS dbSNP
NM_000528.4(MAN2B1):c.*42G>A rs149101136
NM_000528.4(MAN2B1):c.1010G>A (p.Arg337Gln) rs1133330
NM_000528.4(MAN2B1):c.1020T>C (p.Asn340=) rs1389459819
NM_000528.4(MAN2B1):c.1023G>A (p.Ala341=) rs755616565
NM_000528.4(MAN2B1):c.1026+8C>T
NM_000528.4(MAN2B1):c.1026+9G>A rs762829719
NM_000528.4(MAN2B1):c.1027-4G>A rs368900863
NM_000528.4(MAN2B1):c.1027-7C>T
NM_000528.4(MAN2B1):c.1044T>C (p.Ser348=)
NM_000528.4(MAN2B1):c.1056C>T (p.Leu352=)
NM_000528.4(MAN2B1):c.1068C>G (p.Pro356=) rs117880912
NM_000528.4(MAN2B1):c.1068C>T (p.Pro356=)
NM_000528.4(MAN2B1):c.1080C>G (p.Leu360=)
NM_000528.4(MAN2B1):c.1104C>A (p.Leu368=)
NM_000528.4(MAN2B1):c.1109+10G>A
NM_000528.4(MAN2B1):c.1109+41C>A rs200862799
NM_000528.4(MAN2B1):c.1110-4G>A rs758041910
NM_000528.4(MAN2B1):c.1110-4G>T
NM_000528.4(MAN2B1):c.1110-8C>T rs201690866
NM_000528.4(MAN2B1):c.1125C>T (p.Asp375=)
NM_000528.4(MAN2B1):c.1134C>T (p.Phe378=)
NM_000528.4(MAN2B1):c.1158G>A (p.Gln386=) rs112829030
NM_000528.4(MAN2B1):c.1167C>T (p.Thr389=) rs762375074
NM_000528.4(MAN2B1):c.116T>C (p.Leu39Pro)
NM_000528.4(MAN2B1):c.1188G>A (p.Pro396=)
NM_000528.4(MAN2B1):c.1206G>A (p.Glu402=)
NM_000528.4(MAN2B1):c.1209C>A (p.Arg403=) rs559827776
NM_000528.4(MAN2B1):c.1221C>T (p.Asn407=)
NM_000528.4(MAN2B1):c.1231-5T>A rs1419185296
NM_000528.4(MAN2B1):c.1231-5_1231-4dup
NM_000528.4(MAN2B1):c.1231-7C>T
NM_000528.4(MAN2B1):c.1231-8G>T
NM_000528.4(MAN2B1):c.1238A>G (p.Asn413Ser) rs35836657
NM_000528.4(MAN2B1):c.1245G>A (p.Leu415=)
NM_000528.4(MAN2B1):c.1251G>A (p.Ala417=)
NM_000528.4(MAN2B1):c.1252C>T (p.Leu418=)
NM_000528.4(MAN2B1):c.1269C>T (p.Ala423=)
NM_000528.4(MAN2B1):c.1272C>T (p.Asn424=)
NM_000528.4(MAN2B1):c.1278A>T (p.Gly426=) rs950266158
NM_000528.4(MAN2B1):c.1302A>C (p.Ala434=)
NM_000528.4(MAN2B1):c.1309+10G>A rs1424931652
NM_000528.4(MAN2B1):c.1310-7T>C
NM_000528.4(MAN2B1):c.1310-9T>C
NM_000528.4(MAN2B1):c.1329C>A (p.Leu443=)
NM_000528.4(MAN2B1):c.1356C>T (p.Thr452=)
NM_000528.4(MAN2B1):c.135C>G (p.Ala45=) rs200413076
NM_000528.4(MAN2B1):c.1383C>T (p.Tyr461=) rs775200333
NM_000528.4(MAN2B1):c.1398G>A (p.Ala466=) rs774396746
NM_000528.4(MAN2B1):c.1398G>C (p.Ala466=)
NM_000528.4(MAN2B1):c.1398G>T (p.Ala466=) rs774396746
NM_000528.4(MAN2B1):c.1419+7G>C
NM_000528.4(MAN2B1):c.1437G>A (p.Ala479=)
NM_000528.4(MAN2B1):c.1437G>T (p.Ala479=) rs139435774
NM_000528.4(MAN2B1):c.1443G>A (p.Ala481=)
NM_000528.4(MAN2B1):c.1467C>T (p.His489=)
NM_000528.4(MAN2B1):c.1509C>T (p.Leu503=)
NM_000528.4(MAN2B1):c.1518G>A (p.Thr506=) rs754672974
NM_000528.4(MAN2B1):c.1521G>T (p.Ala507=) rs143318498
NM_000528.4(MAN2B1):c.1527+7C>T
NM_000528.4(MAN2B1):c.1528-5C>T
NM_000528.4(MAN2B1):c.1528-8C>T
NM_000528.4(MAN2B1):c.1578A>T (p.Val526=) rs768096085
NM_000528.4(MAN2B1):c.1581G>A (p.Arg527=) rs149613968
NM_000528.4(MAN2B1):c.1587G>T (p.Pro529=) rs771761940
NM_000528.4(MAN2B1):c.159+9G>A rs764391534
NM_000528.4(MAN2B1):c.1590C>T (p.Val530=)
NM_000528.4(MAN2B1):c.1593C>T (p.Ser531=)
NM_000528.4(MAN2B1):c.160-5T>C
NM_000528.4(MAN2B1):c.1605C>T (p.Phe535=)
NM_000528.4(MAN2B1):c.1641C>T (p.Ser547=) rs1295503998
NM_000528.4(MAN2B1):c.1659C>T (p.Pro553=) rs1376701673
NM_000528.4(MAN2B1):c.1662C>T (p.Ser554=)
NM_000528.4(MAN2B1):c.1677G>A (p.Ala559=)
NM_000528.4(MAN2B1):c.16C>A (p.Arg6=)
NM_000528.4(MAN2B1):c.1704C>T (p.Ala568=)
NM_000528.4(MAN2B1):c.1708C>T (p.Leu570=)
NM_000528.4(MAN2B1):c.1713C>T (p.Pro571=) rs747081586
NM_000528.4(MAN2B1):c.1716C>T (p.Ala572=)
NM_000528.4(MAN2B1):c.1717C>T (p.Leu573=)
NM_000528.4(MAN2B1):c.1722C>T (p.Gly574=) rs1599348302
NM_000528.4(MAN2B1):c.1725C>T (p.Phe575=)
NM_000528.4(MAN2B1):c.1773C>T (p.Arg591=)
NM_000528.4(MAN2B1):c.1779A>G (p.Pro593=) rs146778702
NM_000528.4(MAN2B1):c.1782G>A (p.Gln594=)
NM_000528.4(MAN2B1):c.180G>A (p.Pro60=)
NM_000528.4(MAN2B1):c.1818C>T (p.Thr606=)
NM_000528.4(MAN2B1):c.1822G>A (p.Glu608Lys) rs145062583
NM_000528.4(MAN2B1):c.1831-5C>T
NM_000528.4(MAN2B1):c.1838G>A (p.Arg613Gln) rs543222535
NM_000528.4(MAN2B1):c.183C>T (p.Asn61=)
NM_000528.4(MAN2B1):c.1845G>A (p.Thr615=) rs369071579
NM_000528.4(MAN2B1):c.1850A>G (p.Asp617Gly) rs370382032
NM_000528.4(MAN2B1):c.1875G>A (p.Glu625=) rs753652903
NM_000528.4(MAN2B1):c.1902G>A (p.Leu634=)
NM_000528.4(MAN2B1):c.1908T>G (p.Pro636=)
NM_000528.4(MAN2B1):c.1926C>T (p.Phe642=)
NM_000528.4(MAN2B1):c.1928+10G>C rs200579436
NM_000528.4(MAN2B1):c.1932C>T (p.Tyr644=)
NM_000528.4(MAN2B1):c.1953C>T (p.Asn651=)
NM_000528.4(MAN2B1):c.1959T>C (p.Ser653=)
NM_000528.4(MAN2B1):c.2007G>A (p.Pro669=) rs762152042
NM_000528.4(MAN2B1):c.201G>A (p.Leu67=)
NM_000528.4(MAN2B1):c.2034C>A (p.Ile678=)
NM_000528.4(MAN2B1):c.2047-4G>A rs768347546
NM_000528.4(MAN2B1):c.2047-5C>T rs200424566
NM_000528.4(MAN2B1):c.2052C>T (p.Pro684=)
NM_000528.4(MAN2B1):c.2107C>T (p.Leu703=)
NM_000528.4(MAN2B1):c.2112C>T (p.Tyr704=)
NM_000528.4(MAN2B1):c.2127C>T (p.His709=) rs1187915902
NM_000528.4(MAN2B1):c.2154G>C (p.Pro718=)
NM_000528.4(MAN2B1):c.2161G>A (p.Val721Met) rs148134639
NM_000528.4(MAN2B1):c.2165+8G>A
NM_000528.4(MAN2B1):c.2169C>T (p.Asp723=)
NM_000528.4(MAN2B1):c.2193C>T (p.Ser731=)
NM_000528.4(MAN2B1):c.2208G>A (p.Pro736=)
NM_000528.4(MAN2B1):c.2220G>A (p.Lys740=) rs1599341929
NM_000528.4(MAN2B1):c.2221G>A (p.Gly741Arg) rs61234887
NM_000528.4(MAN2B1):c.2226C>T (p.Arg742=)
NM_000528.4(MAN2B1):c.222C>T (p.Asp74=)
NM_000528.4(MAN2B1):c.2247C>T (p.Gly749=)
NM_000528.4(MAN2B1):c.2248C>A (p.Arg750=)
NM_000528.4(MAN2B1):c.2250G>A (p.Arg750=)
NM_000528.4(MAN2B1):c.2253G>A (p.Glu751=)
NM_000528.4(MAN2B1):c.2260G>A (p.Glu754Lys) rs141212446
NM_000528.4(MAN2B1):c.2267+3dup rs572289342
NM_000528.4(MAN2B1):c.2267+8G>T rs1599341786
NM_000528.4(MAN2B1):c.2267+9T>C
NM_000528.4(MAN2B1):c.2283C>T (p.Pro761=) rs138358081
NM_000528.4(MAN2B1):c.228C>T (p.Gly76=)
NM_000528.4(MAN2B1):c.2298C>T (p.Asn766=)
NM_000528.4(MAN2B1):c.2304G>A (p.Thr768=)
NM_000528.4(MAN2B1):c.2349C>T (p.Tyr783=)
NM_000528.4(MAN2B1):c.2355+33C>T rs374660827
NM_000528.4(MAN2B1):c.2355+5C>G rs770412137
NM_000528.4(MAN2B1):c.2356-4C>A
NM_000528.4(MAN2B1):c.2388C>T (p.Asp796=)
NM_000528.4(MAN2B1):c.2404A>G (p.Ser802Gly) rs141391488
NM_000528.4(MAN2B1):c.2409C>T (p.Ser803=) rs147850230
NM_000528.4(MAN2B1):c.2424G>C (p.Ser808=)
NM_000528.4(MAN2B1):c.2436+17C>T rs148420017
NM_000528.4(MAN2B1):c.2436+7G>C
NM_000528.4(MAN2B1):c.2436+8G>C
NM_000528.4(MAN2B1):c.2436+8G>T
NM_000528.4(MAN2B1):c.2437-10C>T
NM_000528.4(MAN2B1):c.2437-4C>G rs772778684
NM_000528.4(MAN2B1):c.2437-5C>A rs200695002
NM_000528.4(MAN2B1):c.2437-5C>G rs200695002
NM_000528.4(MAN2B1):c.2437-6C>T
NM_000528.4(MAN2B1):c.2437-8C>A rs1599339769
NM_000528.4(MAN2B1):c.2469C>T (p.Arg823=)
NM_000528.4(MAN2B1):c.2472A>T (p.Gly824=)
NM_000528.4(MAN2B1):c.2478G>A (p.Ser826=)
NM_000528.4(MAN2B1):c.2485C>T (p.Leu829=)
NM_000528.4(MAN2B1):c.2499G>A (p.Gly833=)
NM_000528.4(MAN2B1):c.2502G>A (p.Ser834=)
NM_000528.4(MAN2B1):c.2529G>A (p.Leu843=)
NM_000528.4(MAN2B1):c.2535G>A (p.Leu845=)
NM_000528.4(MAN2B1):c.2547C>G (p.Ala849=)
NM_000528.4(MAN2B1):c.2559C>G (p.Ala853=)
NM_000528.4(MAN2B1):c.2559C>T (p.Ala853=)
NM_000528.4(MAN2B1):c.2562C>T (p.Ala854=)
NM_000528.4(MAN2B1):c.2571G>T (p.Arg857=)
NM_000528.4(MAN2B1):c.2580G>C (p.Ala860=)
NM_000528.4(MAN2B1):c.2583G>A (p.Glu861=)
NM_000528.4(MAN2B1):c.2592C>T (p.Val864=)
NM_000528.4(MAN2B1):c.2619G>C (p.Pro873=)
NM_000528.4(MAN2B1):c.262+10G>A
NM_000528.4(MAN2B1):c.2622T>C (p.Gly874=)
NM_000528.4(MAN2B1):c.2625C>T (p.Gly875=) rs368834616
NM_000528.4(MAN2B1):c.263-10T>C
NM_000528.4(MAN2B1):c.263-4A>C
NM_000528.4(MAN2B1):c.263-7T>C
NM_000528.4(MAN2B1):c.263-8A>G rs1463660136
NM_000528.4(MAN2B1):c.2640T>C (p.Asn880=) rs763786776
NM_000528.4(MAN2B1):c.2643C>T (p.Leu881=)
NM_000528.4(MAN2B1):c.2655G>A (p.Pro885=)
NM_000528.4(MAN2B1):c.2658C>G (p.Arg886=) rs556554403
NM_000528.4(MAN2B1):c.2661G>A (p.Thr887=)
NM_000528.4(MAN2B1):c.2664+9C>T rs1485817124
NM_000528.4(MAN2B1):c.2665-4G>A rs1461826298
NM_000528.4(MAN2B1):c.2665-5C>T
NM_000528.4(MAN2B1):c.2676G>A (p.Leu892=)
NM_000528.4(MAN2B1):c.2679C>A (p.Arg893=)
NM_000528.4(MAN2B1):c.2686C>T (p.Leu896=)
NM_000528.4(MAN2B1):c.2691G>A (p.Pro897=)
NM_000528.4(MAN2B1):c.2694C>T (p.Pro898=)
NM_000528.4(MAN2B1):c.2748C>T (p.Arg916=) rs1184081650
NM_000528.4(MAN2B1):c.2766C>T (p.Ala922=) rs150866794
NM_000528.4(MAN2B1):c.2782G>A (p.Gly928Arg)
NM_000528.4(MAN2B1):c.2782G>C (p.Gly928Arg) rs754733253
NM_000528.4(MAN2B1):c.2784A>C (p.Gly928=)
NM_000528.4(MAN2B1):c.2799C>T (p.Ala933=)
NM_000528.4(MAN2B1):c.27G>C (p.Gly9=)
NM_000528.4(MAN2B1):c.27G>T (p.Gly9=)
NM_000528.4(MAN2B1):c.2802C>T (p.Pro934=)
NM_000528.4(MAN2B1):c.2820+10G>A
NM_000528.4(MAN2B1):c.2821-5C>T rs761870446
NM_000528.4(MAN2B1):c.2821-9T>C
NM_000528.4(MAN2B1):c.282C>T (p.His94=)
NM_000528.4(MAN2B1):c.2841C>A (p.Thr947=) rs1599338014
NM_000528.4(MAN2B1):c.285C>G (p.Ala95=)
NM_000528.4(MAN2B1):c.285C>T (p.Ala95=) rs750997069
NM_000528.4(MAN2B1):c.2865G>A (p.Thr955=) rs148108322
NM_000528.4(MAN2B1):c.2865G>C (p.Thr955=) rs148108322
NM_000528.4(MAN2B1):c.2877C>T (p.Asn959=)
NM_000528.4(MAN2B1):c.2883C>A (p.Leu961=)
NM_000528.4(MAN2B1):c.2892A>G (p.Ala964=)
NM_000528.4(MAN2B1):c.2913A>G (p.Thr971=)
NM_000528.4(MAN2B1):c.2923+9C>T
NM_000528.4(MAN2B1):c.2924-4C>T
NM_000528.4(MAN2B1):c.2946G>A (p.Pro982=)
NM_000528.4(MAN2B1):c.2952G>A (p.Gln984=)
NM_000528.4(MAN2B1):c.2961G>A (p.Pro987=) rs369658144
NM_000528.4(MAN2B1):c.2973G>A (p.Thr991=) rs148945108
NM_000528.4(MAN2B1):c.2994C>T (p.Arg998=)
NM_000528.4(MAN2B1):c.3033T>C (p.Gly1011=)
NM_000528.4(MAN2B1):c.306C>T (p.Asp102=)
NM_000528.4(MAN2B1):c.309G>T (p.Ser103=) rs1175779934
NM_000528.4(MAN2B1):c.30C>G (p.Val10=)
NM_000528.4(MAN2B1):c.321C>T (p.Ala107=)
NM_000528.4(MAN2B1):c.322T>C (p.Leu108=)
NM_000528.4(MAN2B1):c.325C>T (p.Leu109=) rs756417972
NM_000528.4(MAN2B1):c.33C>T (p.Cys11=) rs1599361566
NM_000528.4(MAN2B1):c.354C>T (p.Tyr118=)
NM_000528.4(MAN2B1):c.366C>G (p.Ala122=)
NM_000528.4(MAN2B1):c.39C>G (p.Arg13=) rs537304777
NM_000528.4(MAN2B1):c.414C>T (p.Val138=)
NM_000528.4(MAN2B1):c.418C>A (p.Arg140=)
NM_000528.4(MAN2B1):c.419G>A (p.Arg140Gln) rs139281846
NM_000528.4(MAN2B1):c.436+7C>T
NM_000528.4(MAN2B1):c.437-6G>A
NM_000528.4(MAN2B1):c.437-8T>C
NM_000528.4(MAN2B1):c.444G>C (p.Leu148=) rs794727626
NM_000528.4(MAN2B1):c.450C>T (p.Phe150=)
NM_000528.4(MAN2B1):c.455A>G (p.Asn152Ser) rs200164758
NM_000528.4(MAN2B1):c.474C>T (p.Asn158=) rs146331898
NM_000528.4(MAN2B1):c.51C>T (p.Asp17=)
NM_000528.4(MAN2B1):c.525G>A (p.Gly175=)
NM_000528.4(MAN2B1):c.526C>T (p.Leu176=)
NM_000528.4(MAN2B1):c.531C>A (p.Arg177=)
NM_000528.4(MAN2B1):c.552C>A (p.Gly184=)
NM_000528.4(MAN2B1):c.591C>T (p.Pro197=)
NM_000528.4(MAN2B1):c.597C>T (p.Gly199=) rs200872797
NM_000528.4(MAN2B1):c.609G>A (p.Glu203=)
NM_000528.4(MAN2B1):c.609G>T (p.Glu203Asp) rs139290127
NM_000528.4(MAN2B1):c.618G>A (p.Ser206=)
NM_000528.4(MAN2B1):c.630+10G>T rs1200800972
NM_000528.4(MAN2B1):c.630+12G>C rs368271384
NM_000528.4(MAN2B1):c.630+29C>T rs144337367
NM_000528.4(MAN2B1):c.630+9C>T
NM_000528.4(MAN2B1):c.631-9C>T
NM_000528.4(MAN2B1):c.642C>T (p.Asp214=) rs755806804
NM_000528.4(MAN2B1):c.660C>T (p.Arg220=)
NM_000528.4(MAN2B1):c.687G>A (p.Arg229=) rs1599357346
NM_000528.4(MAN2B1):c.719G>A (p.Arg240Gln) rs11554970
NM_000528.4(MAN2B1):c.743C>T (p.Pro248Leu) rs117843968
NM_000528.4(MAN2B1):c.744G>A (p.Pro248=) rs3745649
NM_000528.4(MAN2B1):c.763+9C>T
NM_000528.4(MAN2B1):c.789G>A (p.Pro263=) rs149484019
NM_000528.4(MAN2B1):c.810T>C (p.Asp270=)
NM_000528.4(MAN2B1):c.81C>T (p.Ala27=) rs1407475487
NM_000528.4(MAN2B1):c.831G>A (p.Pro277=)
NM_000528.4(MAN2B1):c.832C>G (p.Leu278Val) rs1054486
NM_000528.4(MAN2B1):c.844C>T (p.Pro282Ser) rs45576136
NM_000528.4(MAN2B1):c.855C>T (p.Pro285=) rs139218045
NM_000528.4(MAN2B1):c.861C>T (p.Tyr287=)
NM_000528.4(MAN2B1):c.864C>T (p.Asn288=) rs146909343
NM_000528.4(MAN2B1):c.867C>T (p.Ala289=)
NM_000528.4(MAN2B1):c.874C>T (p.Leu292=) rs141077530
NM_000528.4(MAN2B1):c.876G>A (p.Leu292=)
NM_000528.4(MAN2B1):c.879C>T (p.Val293=)
NM_000528.4(MAN2B1):c.889C>T (p.Leu297=)
NM_000528.4(MAN2B1):c.906C>T (p.Ala302=) rs749372996
NM_000528.4(MAN2B1):c.909+9G>A
NM_000528.4(MAN2B1):c.915G>A (p.Arg305=)
NM_000528.4(MAN2B1):c.915G>T (p.Arg305=) rs755994517
NM_000528.4(MAN2B1):c.921C>T (p.Tyr307=) rs35087690
NM_000528.4(MAN2B1):c.927C>T (p.Thr309=) rs759023914
NM_000528.4(MAN2B1):c.933C>T (p.His311=) rs760393236
NM_000528.4(MAN2B1):c.935C>A (p.Thr312Asn) rs1054487
NM_000528.4(MAN2B1):c.935C>T (p.Thr312Ile) rs1054487
NM_000528.4(MAN2B1):c.966T>C (p.Tyr322=) rs762918325

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