ClinVar Miner

List of variants in gene RAF1 reported as likely benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 81
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.*348T>C rs5746247 0.01554
NM_002880.4(RAF1):c.424-129A>G rs116215412 0.01156
NM_002880.4(RAF1):c.1418-241G>A rs113102168 0.01138
NM_002880.4(RAF1):c.582-137A>G rs61762461 0.01128
NM_002880.3(RAF1):c.-415-1C>G rs61730434 0.01127
NM_002880.4(RAF1):c.208-85C>T rs5746196 0.00768
NM_002880.4(RAF1):c.-27+125C>T rs545433998 0.00713
NM_002880.4(RAF1):c.1108+196A>C rs5746228 0.00610
NM_002880.4(RAF1):c.923C>T (p.Pro308Leu) rs5746220 0.00571
NM_002880.4(RAF1):c.208-316C>T rs541501559 0.00340
NM_002880.4(RAF1):c.*190G>A rs528863135 0.00335
NM_002880.4(RAF1):c.1371-295G>A rs538066384 0.00240
NM_002880.4(RAF1):c.*110T>C rs550188508 0.00112
NM_002880.4(RAF1):c.1830A>G (p.Gln610=) rs141791080 0.00088
NM_002880.4(RAF1):c.-201C>A rs532668125 0.00073
NM_002880.4(RAF1):c.212A>G (p.Asn71Ser) rs184022679 0.00029
NM_002880.4(RAF1):c.909A>C (p.Thr303=) rs5746219 0.00025
NM_002880.4(RAF1):c.125C>T (p.Ala42Val) rs11549992 0.00021
NM_002880.4(RAF1):c.576A>G (p.Gln192=) rs148759910 0.00016
NM_002880.4(RAF1):c.680+6T>C rs371846795 0.00014
NM_002880.4(RAF1):c.94A>G (p.Ile32Val) rs372738063 0.00013
NM_002880.4(RAF1):c.935T>C (p.Val312Ala) rs370243307 0.00010
NM_002880.4(RAF1):c.1107C>T (p.His369=) rs761947194 0.00006
NM_002880.4(RAF1):c.1194-9C>T rs200322423 0.00005
NM_002880.4(RAF1):c.1272C>T (p.Cys424=) rs142942142 0.00005
NM_002880.4(RAF1):c.-47G>A rs1039418534 0.00004
NM_002880.4(RAF1):c.1194-16C>T rs754344039 0.00004
NM_002880.4(RAF1):c.435G>A (p.Thr145=) rs371565419 0.00004
NM_002880.4(RAF1):c.570C>T (p.Ile190=) rs780912024 0.00004
NM_002880.4(RAF1):c.835-9C>G rs200112870 0.00004
NM_002880.4(RAF1):c.1109-17G>C rs770431112 0.00003
NM_002880.4(RAF1):c.1113T>C (p.Asp371=) rs146668293 0.00002
NM_002880.4(RAF1):c.1431T>C (p.His477=) rs770034641 0.00002
NM_002880.4(RAF1):c.873A>G (p.Ser291=) rs139135606 0.00002
NM_002880.4(RAF1):c.934G>A (p.Val312Met) rs555034652 0.00002
NM_002880.4(RAF1):c.1051C>T (p.Leu351=) rs1478388712 0.00001
NM_002880.4(RAF1):c.1247A>G (p.Asn416Ser) rs774198365 0.00001
NM_002880.4(RAF1):c.171T>C (p.Thr57=) rs751571550 0.00001
NM_002880.4(RAF1):c.309C>T (p.His103=) rs1057520880 0.00001
NM_002880.4(RAF1):c.321T>C (p.Gly107=) rs201937982 0.00001
NM_002880.4(RAF1):c.507C>G (p.Gly169=) rs1309333776 0.00001
NM_002880.4(RAF1):c.513A>G (p.Lys171=) rs561163045 0.00001
NM_002880.4(RAF1):c.835G>A (p.Asp279Asn) rs368796800 0.00001
NM_002880.4(RAF1):c.845G>A (p.Arg282Gln) rs752713997 0.00001
NM_002880.4(RAF1):c.855C>T (p.Ser285=) rs763657486 0.00001
NM_002880.4(RAF1):c.924G>A (p.Pro308=) rs551674056 0.00001
NM_002880.4(RAF1):c.93A>G (p.Thr31=) rs762478810 0.00001
NM_002880.4(RAF1):c.*710_*737dup
NM_002880.4(RAF1):c.-204G>C rs547543588
NM_002880.4(RAF1):c.1108+157C>G rs5746227
NM_002880.4(RAF1):c.1109-120G>A rs5746234
NM_002880.4(RAF1):c.1314C>T (p.Thr438=) rs147547744
NM_002880.4(RAF1):c.1371-217_1371-211dup rs374515740
NM_002880.4(RAF1):c.1371-218_1371-217insCAAAAAAAAAAA rs1553610554
NM_002880.4(RAF1):c.1537-11_1537-3dup rs730880996
NM_002880.4(RAF1):c.1629G>A (p.Thr543=) rs5746244
NM_002880.4(RAF1):c.1668+10_1668+11del rs730880997
NM_002880.4(RAF1):c.1668+19G>T rs5746245
NM_002880.4(RAF1):c.1698C>T (p.Ala566=) rs1559399013
NM_002880.4(RAF1):c.1704A>G (p.Pro568=) rs1575530495
NM_002880.4(RAF1):c.1824G>A (p.Leu608=) rs1057523409
NM_002880.4(RAF1):c.1842G>C (p.Pro614=) rs200235582
NM_002880.4(RAF1):c.208-315C>G rs575996625
NM_002880.4(RAF1):c.21T>C (p.Ala7=) rs886057915
NM_002880.4(RAF1):c.309C>G (p.His103Gln) rs1057520880
NM_002880.4(RAF1):c.399T>C (p.His133=) rs747303896
NM_002880.4(RAF1):c.423+12A>T rs1055790600
NM_002880.4(RAF1):c.435G>T (p.Thr145=) rs371565419
NM_002880.4(RAF1):c.475C>T (p.Leu159=) rs1169686054
NM_002880.4(RAF1):c.60C>T (p.Ala20=) rs755869970
NM_002880.4(RAF1):c.627A>C (p.Leu209=) rs759564229
NM_002880.4(RAF1):c.681-248T>C rs5746209
NM_002880.4(RAF1):c.681-5C>G rs1057523180
NM_002880.4(RAF1):c.835-1599G>T
NM_002880.4(RAF1):c.835-225T>G
NM_002880.4(RAF1):c.835-362C>T
NM_002880.4(RAF1):c.835-505C>G
NM_002880.4(RAF1):c.835-53dup rs5746218
NM_002880.4(RAF1):c.868_870delinsACC (p.Pro290Thr) rs2125380943
NM_002880.4(RAF1):c.873A>T (p.Ser291=) rs139135606
NM_002880.4(RAF1):c.991-11A>G rs1057522961

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.