ClinVar Miner

List of variants in gene FANCB studied for abdominal and pelvic region disorder

Included ClinVar conditions (1042):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 150
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HGVS dbSNP
FANCB, 1-BP DEL, 1650T
FANCB, 1-BP INS, 1838T
FANCB, 1-BP INS, 811T
FANCB, 3314-BP DEL
NC_000023.11:g.(?_14843557)_(14873062_?)dup
NC_000023.11:g.(?_14857852)_(14859344_?)del
NC_000023.11:g.14843408_14873063del
NC_000023.11:g.14864560_14869043dup
NM_001018113.3(FANCB):c.*14T>C rs2375726
NM_001018113.3(FANCB):c.*151A>G
NM_001018113.3(FANCB):c.*33T>C rs187611308
NM_001018113.3(FANCB):c.*66T>G rs143434225
NM_001018113.3(FANCB):c.-111A>G
NM_001018113.3(FANCB):c.-173G>C rs2188383
NM_001018113.3(FANCB):c.-219G>T
NM_001018113.3(FANCB):c.-229T>G rs149617434
NM_001018113.3(FANCB):c.-230A>T rs1020271259
NM_001018113.3(FANCB):c.-232G>A rs756766337
NM_001018113.3(FANCB):c.1004G>A (p.Gly335Glu) rs41309679
NM_001018113.3(FANCB):c.1067C>T (p.Ser356Leu) rs142304943
NM_001018113.3(FANCB):c.1078A>G (p.Thr360Ala) rs956498867
NM_001018113.3(FANCB):c.1079C>T (p.Thr360Met) rs138192474
NM_001018113.3(FANCB):c.1103C>A (p.Ser368Ter) rs143585647
NM_001018113.3(FANCB):c.1104+4A>G rs1555906676
NM_001018113.3(FANCB):c.1105-26TATT[5] rs398123537
NM_001018113.3(FANCB):c.1105-26TATT[7] rs398123537
NM_001018113.3(FANCB):c.1133A>C (p.Asp378Ala) rs1569088991
NM_001018113.3(FANCB):c.1140T>A (p.Phe380Leu) rs199909156
NM_001018113.3(FANCB):c.1179T>C (p.Pro393=)
NM_001018113.3(FANCB):c.1265C>T (p.Ser422Phe) rs1057515805
NM_001018113.3(FANCB):c.1288G>A (p.Val430Ile) rs1018343095
NM_001018113.3(FANCB):c.128T>C (p.Leu43Ser) rs1602006737
NM_001018113.3(FANCB):c.1310C>T (p.Thr437Met) rs772802668
NM_001018113.3(FANCB):c.131A>C (p.His44Pro)
NM_001018113.3(FANCB):c.1325A>C (p.Glu442Ala)
NM_001018113.3(FANCB):c.1327-10T>C rs2905223
NM_001018113.3(FANCB):c.1327-3del rs202067682
NM_001018113.3(FANCB):c.1331A>T (p.Glu444Val) rs368679125
NM_001018113.3(FANCB):c.1342C>T (p.Pro448Ser) rs867778700
NM_001018113.3(FANCB):c.1349G>A (p.Cys450Tyr) rs764817410
NM_001018113.3(FANCB):c.1371C>T (p.Val457=) rs149695930
NM_001018113.3(FANCB):c.1372C>T (p.His458Tyr) rs1601985554
NM_001018113.3(FANCB):c.1442G>A (p.Arg481His) rs140198444
NM_001018113.3(FANCB):c.1487C>T (p.Ser496Phe) rs993307430
NM_001018113.3(FANCB):c.1494G>T (p.Lys498Asn) rs199510538
NM_001018113.3(FANCB):c.1496+5G>A rs1569085810
NM_001018113.3(FANCB):c.1497_2580del (p.Ser500fs)
NM_001018113.3(FANCB):c.1541A>G (p.His514Arg) rs1555904475
NM_001018113.3(FANCB):c.1570C>G (p.Gln524Glu) rs370248837
NM_001018113.3(FANCB):c.1605C>G (p.Phe535Leu) rs1555904458
NM_001018113.3(FANCB):c.1606C>T (p.Pro536Ser)
NM_001018113.3(FANCB):c.1638A>T (p.Gly546=) rs753355273
NM_001018113.3(FANCB):c.1652G>A (p.Arg551Lys)
NM_001018113.3(FANCB):c.1655T>C (p.Val552Ala) rs1569083698
NM_001018113.3(FANCB):c.1658C>T (p.Thr553Met) rs146157131
NM_001018113.3(FANCB):c.1659G>A (p.Thr553=) rs767952529
NM_001018113.3(FANCB):c.1664C>T (p.Thr555Ile)
NM_001018113.3(FANCB):c.1668del (p.Asp557fs) rs1569083679
NM_001018113.3(FANCB):c.1702C>T (p.His568Tyr)
NM_001018113.3(FANCB):c.1707A>G (p.Pro569=) rs1555904427
NM_001018113.3(FANCB):c.1719G>T (p.Glu573Asp)
NM_001018113.3(FANCB):c.1720T>A (p.Cys574Ser) rs200303151
NM_001018113.3(FANCB):c.1769T>C (p.Phe590Ser) rs142959373
NM_001018113.3(FANCB):c.1785C>G (p.Cys595Trp)
NM_001018113.3(FANCB):c.1807_1808GA[2] (p.Arg604fs) rs1601977912
NM_001018113.3(FANCB):c.1817G>A (p.Ser606Asn) rs148560784
NM_001018113.3(FANCB):c.1838G>A (p.Arg613His) rs144764663
NM_001018113.3(FANCB):c.183C>T (p.Ser61=)
NM_001018113.3(FANCB):c.1855_1856AG[1] (p.Arg619fs) rs1569083464
NM_001018113.3(FANCB):c.1856_1857insT (p.Arg619fs) rs1601977844
NM_001018113.3(FANCB):c.1929G>A (p.Glu643=)
NM_001018113.3(FANCB):c.1957G>A (p.Ala653Thr)
NM_001018113.3(FANCB):c.195dup (p.Thr66fs) rs1602006627
NM_001018113.3(FANCB):c.196A>C (p.Thr66Pro)
NM_001018113.3(FANCB):c.1972T>A (p.Ser658Thr)
NM_001018113.3(FANCB):c.1987A>G (p.Thr663Ala) rs184796918
NM_001018113.3(FANCB):c.1991C>T (p.Ser664Leu) rs1555904350
NM_001018113.3(FANCB):c.1995C>T (p.Pro665=) rs192743430
NM_001018113.3(FANCB):c.1996G>A (p.Gly666Ser) rs145110602
NM_001018113.3(FANCB):c.199A>G (p.Ile67Val) rs761346761
NM_001018113.3(FANCB):c.2019G>C (p.Lys673Asn)
NM_001018113.3(FANCB):c.2027T>C (p.Leu676Pro) rs1601977531
NM_001018113.3(FANCB):c.2059G>T (p.Glu687Ter) rs1601977510
NM_001018113.3(FANCB):c.2090C>T (p.Pro697Leu) rs147255018
NM_001018113.3(FANCB):c.2098T>C (p.Phe700Leu) rs1232355920
NM_001018113.3(FANCB):c.2107A>T (p.Thr703Ser)
NM_001018113.3(FANCB):c.2117C>T (p.Thr706Ile) rs1278850689
NM_001018113.3(FANCB):c.2125C>G (p.Gln709Glu) rs1060501875
NM_001018113.3(FANCB):c.2150T>G (p.Leu717Ter) rs1569083185
NM_001018113.3(FANCB):c.2154A>G (p.Ile718Met)
NM_001018113.3(FANCB):c.2165+10A>T rs184385334
NM_001018113.3(FANCB):c.2165+1G>T rs1601977379
NM_001018113.3(FANCB):c.2168A>G (p.Asn723Ser) rs1300715683
NM_001018113.3(FANCB):c.2172_2175del (p.Thr725fs) rs1601976655
NM_001018113.3(FANCB):c.2249_2252del (p.Gly750fs) rs1601976527
NM_001018113.3(FANCB):c.2267T>C (p.Ile756Thr) rs756392097
NM_001018113.3(FANCB):c.2311A>G (p.Ser771Gly) rs750381270
NM_001018113.3(FANCB):c.2327C>T (p.Ala776Val) rs761492600
NM_001018113.3(FANCB):c.2342A>G (p.Glu781Gly) rs140363445
NM_001018113.3(FANCB):c.235T>C (p.Cys79Arg) rs879254329
NM_001018113.3(FANCB):c.2373C>T (p.Ser791=)
NM_001018113.3(FANCB):c.2379A>G (p.Gly793=) rs1374912480
NM_001018113.3(FANCB):c.2394C>T (p.Val798=) rs190579053
NM_001018113.3(FANCB):c.2411A>G (p.Asp804Gly) rs148257882
NM_001018113.3(FANCB):c.2420A>C (p.Glu807Ala) rs1020168794
NM_001018113.3(FANCB):c.2452A>G (p.Arg818Gly) rs143131218
NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met) rs201436396
NM_001018113.3(FANCB):c.256A>G (p.Arg86Gly)
NM_001018113.3(FANCB):c.262G>A (p.Gly88Arg) rs142101123
NM_001018113.3(FANCB):c.30C>A (p.Asn10Lys) rs750078094
NM_001018113.3(FANCB):c.30C>G (p.Asn10Lys)
NM_001018113.3(FANCB):c.330A>C (p.Leu110=) rs201633684
NM_001018113.3(FANCB):c.350A>C (p.Lys117Thr) rs1057515811
NM_001018113.3(FANCB):c.357A>T (p.Glu119Asp) rs970828551
NM_001018113.3(FANCB):c.362G>A (p.Arg121His)
NM_001018113.3(FANCB):c.388A>G (p.Met130Val) rs776724055
NM_001018113.3(FANCB):c.402A>G (p.Leu134=) rs147260208
NM_001018113.3(FANCB):c.458T>A (p.Ile153Asn)
NM_001018113.3(FANCB):c.477A>C (p.Lys159Asn) rs1569092592
NM_001018113.3(FANCB):c.504C>G (p.Ser168=) rs373738816
NM_001018113.3(FANCB):c.507T>C (p.Ser169=) rs149609970
NM_001018113.3(FANCB):c.508A>G (p.Ile170Val)
NM_001018113.3(FANCB):c.510T>G (p.Ile170Met) rs775216604
NM_001018113.3(FANCB):c.513G>A (p.Gln171=) rs763353362
NM_001018113.3(FANCB):c.52T>C (p.Tyr18His) rs996732250
NM_001018113.3(FANCB):c.552G>A (p.Leu184=) rs771998496
NM_001018113.3(FANCB):c.587G>A (p.Cys196Tyr) rs1366041068
NM_001018113.3(FANCB):c.652G>C (p.Glu218Gln) rs747819351
NM_001018113.3(FANCB):c.688C>T (p.Pro230Ser)
NM_001018113.3(FANCB):c.69T>C (p.Leu23=) rs151173533
NM_001018113.3(FANCB):c.716A>T (p.Tyr239Phe) rs1555907444
NM_001018113.3(FANCB):c.741C>A (p.Ile247=) rs760773732
NM_001018113.3(FANCB):c.755_767del (p.Leu252fs) rs1602005463
NM_001018113.3(FANCB):c.782G>A (p.Arg261Gln) rs1057515809
NM_001018113.3(FANCB):c.7A>G (p.Ser3Gly) rs139111718
NM_001018113.3(FANCB):c.801A>C (p.Ser267=) rs773005941
NM_001018113.3(FANCB):c.809A>G (p.Asn270Ser)
NM_001018113.3(FANCB):c.829dup (p.Cys277fs) rs1602005335
NM_001018113.3(FANCB):c.833A>G (p.Gln278Arg) rs150435015
NM_001018113.3(FANCB):c.869T>C (p.Met290Thr) rs754552650
NM_001018113.3(FANCB):c.884G>A (p.Gly295Glu) rs1270593506
NM_001018113.3(FANCB):c.897C>T (p.Phe299=) rs753443421
NM_001018113.3(FANCB):c.898G>T (p.Val300Phe) rs757610875
NM_001018113.3(FANCB):c.914C>A (p.Ser305Tyr) rs1057515808
NM_001018113.3(FANCB):c.923C>T (p.Ala308Val) rs1242186487
NM_001018113.3(FANCB):c.949C>T (p.Gln317Ter) rs1602005062
NM_001018113.3(FANCB):c.952-13C>T rs1057515807
NM_001018113.3(FANCB):c.960T>G (p.Ala320=) rs139045247
NM_001018113.3(FANCB):c.986T>C (p.Leu329Pro) rs1161918267
NM_001018113.3(FANCB):c.989T>C (p.Ile330Thr) rs200161949

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