ClinVar Miner

List of variants in gene RAF1 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 117
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln) rs145611571 0.00016
NM_002880.4(RAF1):c.680+6T>C rs371846795 0.00014
NM_002880.4(RAF1):c.1721A>G (p.Tyr574Cys) rs370242565 0.00012
NM_002880.4(RAF1):c.834+598G>A rs375404697 0.00009
NM_002880.4(RAF1):c.365T>C (p.Ile122Thr) rs730881000 0.00007
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe) rs730881004 0.00006
NM_002880.4(RAF1):c.1663G>C (p.Asp555His) rs371704292 0.00004
NM_002880.4(RAF1):c.1913C>T (p.Thr638Met) rs730881007 0.00004
NM_002880.4(RAF1):c.853A>G (p.Ser285Gly) rs150054973 0.00004
NM_002880.4(RAF1):c.1879C>T (p.Arg627Trp) rs730881005 0.00003
NM_002880.4(RAF1):c.1921A>G (p.Thr641Ala) rs1183812590 0.00003
NM_002880.4(RAF1):c.1113T>C (p.Asp371=) rs146668293 0.00002
NM_002880.4(RAF1):c.1668+4A>G rs771344560 0.00002
NM_002880.4(RAF1):c.293T>C (p.Val98Ala) rs763559779 0.00002
NM_002880.4(RAF1):c.313C>G (p.His105Asp) rs397516818 0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=) rs397516823 0.00002
NM_002880.4(RAF1):c.917C>T (p.Ser306Leu) rs886041231 0.00002
NM_002880.4(RAF1):c.934G>A (p.Val312Met) rs555034652 0.00002
NM_002880.4(RAF1):c.1050G>T (p.Met350Ile) rs368860450 0.00001
NM_002880.4(RAF1):c.1067G>C (p.Gly356Ala) rs1357778828 0.00001
NM_002880.4(RAF1):c.1075T>C (p.Ser359Pro) rs765433002 0.00001
NM_002880.4(RAF1):c.1150C>G (p.Pro384Ala) rs140788943 0.00001
NM_002880.4(RAF1):c.1297C>G (p.Leu433Val) rs368676608 0.00001
NM_002880.4(RAF1):c.1553G>A (p.Arg518Gln) rs149580968 0.00001
NM_002880.4(RAF1):c.1685G>T (p.Gly562Val) rs746937683 0.00001
NM_002880.4(RAF1):c.1688G>A (p.Arg563Gln) rs727504827 0.00001
NM_002880.4(RAF1):c.1850A>G (p.Asn617Ser) rs933142627 0.00001
NM_002880.4(RAF1):c.1904A>G (p.Asn635Ser) rs772585174 0.00001
NM_002880.4(RAF1):c.1922C>T (p.Thr641Met) rs587777587 0.00001
NM_002880.4(RAF1):c.1939G>A (p.Val647Ile) rs730881008 0.00001
NM_002880.4(RAF1):c.236A>G (p.His79Arg) rs1387880716 0.00001
NM_002880.4(RAF1):c.262G>T (p.Val88Leu) rs1559438429 0.00001
NM_002880.4(RAF1):c.29C>T (p.Thr10Met) rs144637992 0.00001
NM_002880.4(RAF1):c.41G>A (p.Gly14Asp) rs757333753 0.00001
NM_002880.4(RAF1):c.462C>G (p.Ile154Met) rs367732360 0.00001
NM_002880.4(RAF1):c.601A>G (p.Ile201Val) rs757700986 0.00001
NM_002880.4(RAF1):c.679A>G (p.Ser227Gly) rs730881001 0.00001
NM_002880.4(RAF1):c.683C>G (p.Ser228Cys) rs766437069 0.00001
NM_002880.4(RAF1):c.709G>A (p.Ala237Thr) rs587777588 0.00001
NM_002880.4(RAF1):c.70G>A (p.Gly24Ser) rs1019217338 0.00001
NM_002880.4(RAF1):c.928A>G (p.Thr310Ala) rs778155315 0.00001
NM_002880.4(RAF1):c.997C>T (p.Arg333Cys) rs551466727 0.00001
NM_002880.4(RAF1):c.1178A>C (p.Glu393Ala) rs886042569
NM_002880.4(RAF1):c.1193G>T (p.Arg398Leu) rs730880382
NM_002880.4(RAF1):c.1202G>A (p.Arg401Gln) rs2125343625
NM_002880.4(RAF1):c.121C>T (p.Arg41Trp) rs1480507957
NM_002880.4(RAF1):c.122G>T (p.Arg41Leu) rs145611571
NM_002880.4(RAF1):c.1243G>A (p.Asp415Asn) rs201553362
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile) rs876657965
NM_002880.4(RAF1):c.1323G>T (p.Gln441His) rs1131691942
NM_002880.4(RAF1):c.1338T>G (p.Ile446Met)
NM_002880.4(RAF1):c.1349G>A (p.Arg450Gln) rs886041642
NM_002880.4(RAF1):c.1396C>T (p.His466Tyr) rs886041423
NM_002880.4(RAF1):c.1418A>G (p.Asn473Ser)
NM_002880.4(RAF1):c.1448A>T (p.Lys483Ile) rs2125326352
NM_002880.4(RAF1):c.1453G>A (p.Gly485Arg) rs2125326317
NM_002880.4(RAF1):c.1520G>A (p.Gly507Asp) rs2058312255
NM_002880.4(RAF1):c.1535T>C (p.Met512Thr) rs886042042
NM_002880.4(RAF1):c.1546G>A (p.Val516Met) rs2125323061
NM_002880.4(RAF1):c.1609G>A (p.Val537Ile) rs751232720
NM_002880.4(RAF1):c.1613T>A (p.Leu538Ter) rs730881011
NM_002880.4(RAF1):c.1629G>C (p.Thr543=) rs5746244
NM_002880.4(RAF1):c.1654AAC[1] (p.Asn553del) rs1455454651
NM_002880.4(RAF1):c.1655A>G (p.Asn552Ser) rs775817988
NM_002880.4(RAF1):c.1678A>C (p.Met560Leu) rs754942031
NM_002880.4(RAF1):c.1711A>G (p.Ser571Gly) rs2125319809
NM_002880.4(RAF1):c.1742T>C (p.Met581Thr) rs2125319605
NM_002880.4(RAF1):c.1752G>A (p.Leu584=) rs1064797291
NM_002880.4(RAF1):c.176G>A (p.Arg59His) rs1559447623
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn) rs773583951
NM_002880.4(RAF1):c.1777_1782del (p.Lys593_Glu594del)
NM_002880.4(RAF1):c.1802A>G (p.Gln601Arg) rs1398402832
NM_002880.4(RAF1):c.183C>G (p.Phe61Leu)
NM_002880.4(RAF1):c.1867C>T (p.Pro623Ser) rs373596121
NM_002880.4(RAF1):c.1871C>G (p.Ser624Cys) rs1057524239
NM_002880.4(RAF1):c.1876_1877insTC (p.His626fs)
NM_002880.4(RAF1):c.1880G>A (p.Arg627Gln) rs730881006
NM_002880.4(RAF1):c.1897G>A (p.Asp633Asn) rs1352545039
NM_002880.4(RAF1):c.1936C>T (p.Pro646Ser) rs1060503152
NM_002880.4(RAF1):c.1947G>C (p.Ter649Tyr) rs1471833190
NM_002880.4(RAF1):c.196del (p.Gln66fs) rs2125452707
NM_002880.4(RAF1):c.207+5G>T rs1446781544
NM_002880.4(RAF1):c.208-4G>T rs751334223
NM_002880.4(RAF1):c.20C>G (p.Ala7Gly) rs200365094
NM_002880.4(RAF1):c.212A>T (p.Asn71Ile) rs184022679
NM_002880.4(RAF1):c.226A>G (p.Met76Val) rs730880999
NM_002880.4(RAF1):c.261G>C (p.Lys87Asn) rs2059225407
NM_002880.4(RAF1):c.276A>T (p.Gln92His)
NM_002880.4(RAF1):c.278C>T (p.Pro93Leu) rs1559438381
NM_002880.4(RAF1):c.321-13dup rs2125421223
NM_002880.4(RAF1):c.325_327del (p.Lys109del) rs1418886913
NM_002880.4(RAF1):c.34A>G (p.Ser12Gly) rs2125453642
NM_002880.4(RAF1):c.419A>G (p.Asn140Ser) rs876657968
NM_002880.4(RAF1):c.438C>A (p.Phe146Leu) rs794727717
NM_002880.4(RAF1):c.445C>T (p.Leu149Phe) rs1559433480
NM_002880.4(RAF1):c.453C>A (p.Phe151Leu) rs2125416996
NM_002880.4(RAF1):c.481A>C (p.Asn161His) rs1559433373
NM_002880.4(RAF1):c.512A>C (p.Lys171Thr)
NM_002880.4(RAF1):c.512A>G (p.Lys171Arg) rs876657969
NM_002880.4(RAF1):c.562A>C (p.Ser188Arg) rs886041230
NM_002880.4(RAF1):c.611G>T (p.Ser204Ile) rs756643623
NM_002880.4(RAF1):c.62T>C (p.Val21Ala) rs1306287046
NM_002880.4(RAF1):c.647G>A (p.Arg216His) rs761703202
NM_002880.4(RAF1):c.698C>T (p.Ser233Phe) rs2125398634
NM_002880.4(RAF1):c.708C>G (p.His236Gln) rs370658857
NM_002880.4(RAF1):c.728C>G (p.Ser243Cys) rs1575573477
NM_002880.4(RAF1):c.784A>T (p.Asn262Tyr) rs1575573204
NM_002880.4(RAF1):c.78C>G (p.Ser26Arg) rs886041229
NM_002880.4(RAF1):c.802A>G (p.Thr268Ala) rs1553613743
NM_002880.4(RAF1):c.826A>G (p.Met276Val) rs1189618862
NM_002880.4(RAF1):c.830T>G (p.Ile277Ser) rs1559425852
NM_002880.4(RAF1):c.841A>G (p.Ile281Val)
NM_002880.4(RAF1):c.844C>G (p.Arg282Gly) rs755926381
NM_002880.4(RAF1):c.856G>A (p.Glu286Lys) rs147453956
NM_002880.4(RAF1):c.87_88del (p.Pro30fs) rs1553616654
NM_002880.4(RAF1):c.934G>C (p.Val312Leu) rs555034652
NM_002880.4(RAF1):c.950A>G (p.Glu317Gly)

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.