ClinVar Miner

List of variants in gene combination IFNAR2-IL10RB, IL10RB reported as likely benign for Inflammatory bowel disease 25

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 80
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000628.5(IL10RB):c.73G>A (p.Glu25Lys) rs80027572 0.00286
NM_000628.5(IL10RB):c.442G>A (p.Val148Met) rs45545138 0.00125
NM_000628.5(IL10RB):c.388C>T (p.Arg130Cys) rs138134904 0.00020
NM_000628.5(IL10RB):c.215C>T (p.Thr72Met) rs148466782 0.00019
NM_000628.5(IL10RB):c.630G>A (p.Glu210=) rs374589516 0.00016
NM_000628.5(IL10RB):c.763G>A (p.Ala255Thr) rs182875134 0.00016
NM_000628.5(IL10RB):c.804+17G>A rs369971241 0.00016
NM_000628.5(IL10RB):c.131C>T (p.Ala44Val) rs182073431 0.00014
NM_000628.5(IL10RB):c.647-16C>G rs551931064 0.00014
NM_000628.5(IL10RB):c.954G>A (p.Pro318=) rs374161818 0.00014
NM_000628.5(IL10RB):c.123G>A (p.Glu41=) rs140495014 0.00013
NM_000628.5(IL10RB):c.804+8G>A rs112943706 0.00007
NM_000628.5(IL10RB):c.735G>A (p.Leu245=) rs747586675 0.00006
NM_000628.5(IL10RB):c.762C>T (p.Tyr254=) rs143116323 0.00005
NM_000628.5(IL10RB):c.332-5del rs746600389 0.00004
NM_000628.5(IL10RB):c.50-4A>G rs377541013 0.00004
NM_000628.5(IL10RB):c.717C>T (p.Leu239=) rs755556416 0.00003
NM_000628.5(IL10RB):c.432T>A (p.Thr144=) rs539389729 0.00002
NM_000628.5(IL10RB):c.768C>T (p.Phe256=) rs1427524440 0.00002
NM_000628.5(IL10RB):c.822T>C (p.His274=) rs146668107 0.00002
NM_000628.5(IL10RB):c.891C>T (p.Val297=) rs373486817 0.00002
NM_000628.5(IL10RB):c.132T>A (p.Ala44=) rs1989014876 0.00001
NM_000628.5(IL10RB):c.174-18A>G rs779105633 0.00001
NM_000628.5(IL10RB):c.207T>C (p.Thr69=) rs968662142 0.00001
NM_000628.5(IL10RB):c.259T>C (p.Leu87=) rs201664974 0.00001
NM_000628.5(IL10RB):c.420C>T (p.Tyr140=) rs765588235 0.00001
NM_000628.5(IL10RB):c.647-14A>C rs45526732 0.00001
NM_000628.5(IL10RB):c.657C>T (p.Pro219=) rs1237354106 0.00001
NM_000628.5(IL10RB):c.681C>T (p.Leu227=) rs766067976 0.00001
NM_000628.5(IL10RB):c.690G>A (p.Ser230=) rs751559892 0.00001
NM_000628.5(IL10RB):c.966G>T (p.Gly322=) rs780187887 0.00001
NM_000628.5(IL10RB):c.138C>T (p.Ala46=)
NM_000628.5(IL10RB):c.138_139inv (p.Lys47Glu)
NM_000628.5(IL10RB):c.144G>A (p.Gly48=)
NM_000628.5(IL10RB):c.144G>C (p.Gly48=) rs886965637
NM_000628.5(IL10RB):c.147C>T (p.Asn49=) rs781729452
NM_000628.5(IL10RB):c.150G>A (p.Leu50=)
NM_000628.5(IL10RB):c.174-14T>C rs200472684
NM_000628.5(IL10RB):c.177T>C (p.Tyr59=) rs2096478505
NM_000628.5(IL10RB):c.312C>T (p.Thr104=) rs2123573940
NM_000628.5(IL10RB):c.332-11C>G rs531765635
NM_000628.5(IL10RB):c.332-11C>T rs531765635
NM_000628.5(IL10RB):c.332-17del
NM_000628.5(IL10RB):c.332-7del
NM_000628.5(IL10RB):c.360A>G (p.Val120=) rs1989246111
NM_000628.5(IL10RB):c.372T>G (p.Ala124=)
NM_000628.5(IL10RB):c.444G>A (p.Val148=)
NM_000628.5(IL10RB):c.444G>C (p.Val148=)
NM_000628.5(IL10RB):c.450C>T (p.Asn150=)
NM_000628.5(IL10RB):c.498+19A>G
NM_000628.5(IL10RB):c.50-15G>A
NM_000628.5(IL10RB):c.50-20T>C
NM_000628.5(IL10RB):c.51A>G (p.Ala17=)
NM_000628.5(IL10RB):c.52T>C (p.Leu18=)
NM_000628.5(IL10RB):c.549A>G (p.Pro183=)
NM_000628.5(IL10RB):c.555A>G (p.Thr185=)
NM_000628.5(IL10RB):c.561T>C (p.Tyr187=)
NM_000628.5(IL10RB):c.594G>A (p.Arg198=)
NM_000628.5(IL10RB):c.636A>C (p.Thr212=)
NM_000628.5(IL10RB):c.646+14T>C
NM_000628.5(IL10RB):c.646+19C>T
NM_000628.5(IL10RB):c.647-17C>T
NM_000628.5(IL10RB):c.660C>G (p.Ser220=)
NM_000628.5(IL10RB):c.672C>T (p.Ala224=)
NM_000628.5(IL10RB):c.702C>T (p.Val234=)
NM_000628.5(IL10RB):c.726C>T (p.Phe242=)
NM_000628.5(IL10RB):c.727G>T (p.Ala243Ser) rs1058861
NM_000628.5(IL10RB):c.72C>T (p.Pro24=) rs759657610
NM_000628.5(IL10RB):c.741C>T (p.Cys247=)
NM_000628.5(IL10RB):c.759G>A (p.Lys253=)
NM_000628.5(IL10RB):c.796C>T (p.Leu266=)
NM_000628.5(IL10RB):c.804+12G>A
NM_000628.5(IL10RB):c.804+13G>A
NM_000628.5(IL10RB):c.831A>G (p.Thr277=)
NM_000628.5(IL10RB):c.834T>A (p.Leu278=)
NM_000628.5(IL10RB):c.849T>C (p.Phe283=)
NM_000628.5(IL10RB):c.888T>C (p.Ser296=) rs2082965544
NM_000628.5(IL10RB):c.912C>T (p.Ser304=)
NM_000628.5(IL10RB):c.945C>T (p.Leu315=)
NM_000628.5(IL10RB):c.966G>A (p.Gly322=) rs780187887

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.