ClinVar Miner

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

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Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.991-42T>C rs5746226 0.00943
NM_002880.4(RAF1):c.991-43T>C rs5746225 0.00943
NM_002880.4(RAF1):c.923C>T (p.Pro308Leu) rs5746220 0.00571
NM_002880.4(RAF1):c.681-37C>T rs191998453 0.00215
NM_002880.4(RAF1):c.1830A>G (p.Gln610=) rs141791080 0.00088
NM_002880.4(RAF1):c.581+4A>G rs201776526 0.00087
NM_002880.4(RAF1):c.-59C>A rs201603517 0.00032
NM_002880.4(RAF1):c.909A>C (p.Thr303=) rs5746219 0.00025
NM_002880.4(RAF1):c.122G>A (p.Arg41Gln) rs145611571 0.00016
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.1721A>G (p.Tyr574Cys) rs370242565 0.00012
NM_002880.4(RAF1):c.935T>C (p.Val312Ala) rs370243307 0.00010
NM_002880.4(RAF1):c.1515T>C (p.Pro505=) rs140668986 0.00007
NM_002880.4(RAF1):c.66T>G (p.Phe22Leu) rs397516824 0.00006
NM_002880.4(RAF1):c.1272C>T (p.Cys424=) rs142942142 0.00005
NM_002880.4(RAF1):c.1913C>T (p.Thr638Met) rs730881007 0.00004
NM_002880.4(RAF1):c.435G>A (p.Thr145=) rs371565419 0.00004
NM_002880.4(RAF1):c.863-16T>C rs770891566 0.00004
NM_002880.4(RAF1):c.990+15C>T rs373980711 0.00004
NM_002880.4(RAF1):c.-50G>T rs919436803 0.00003
NM_002880.4(RAF1):c.1108+15C>T rs727503383 0.00003
NM_002880.4(RAF1):c.1821G>A (p.Glu607=) rs747437834 0.00003
NM_002880.4(RAF1):c.600T>C (p.Thr200=) rs779808613 0.00003
NM_002880.4(RAF1):c.63G>A (p.Val21=) rs377377296 0.00003
NM_002880.4(RAF1):c.1431T>C (p.His477=) rs770034641 0.00002
NM_002880.4(RAF1):c.1608C>T (p.Ile536=) rs542779722 0.00002
NM_002880.4(RAF1):c.1669-14T>C rs1260935888 0.00002
NM_002880.4(RAF1):c.639T>C (p.Thr213=) rs397516823 0.00002
NM_002880.4(RAF1):c.934G>A (p.Val312Met) rs555034652 0.00002
NM_002880.4(RAF1):c.945A>G (p.Gln315=) rs1451849309 0.00002
NM_001354689.3(RAF1):c.1200C>T (p.Val400=) rs397516814 0.00001
NM_002880.3(RAF1):c.-382A>G rs397516812 0.00001
NM_002880.4(RAF1):c.*2T>G rs730880998 0.00001
NM_002880.4(RAF1):c.-169G>A rs727504398 0.00001
NM_002880.4(RAF1):c.1656C>T (p.Asn552=) rs772194284 0.00001
NM_002880.4(RAF1):c.1668+14G>C rs1057520886 0.00001
NM_002880.4(RAF1):c.1668+18C>T rs755924543 0.00001
NM_002880.4(RAF1):c.1689A>G (p.Arg563=) rs1358420019 0.00001
NM_002880.4(RAF1):c.171T>C (p.Thr57=) rs751571550 0.00001
NM_002880.4(RAF1):c.321T>C (p.Gly107=) rs201937982 0.00001
NM_002880.4(RAF1):c.391C>T (p.Leu131=) rs878854566 0.00001
NM_002880.4(RAF1):c.471A>G (p.Lys157=) rs1001494773 0.00001
NM_002880.4(RAF1):c.708C>T (p.His236=) rs370658857 0.00001
NM_002880.4(RAF1):c.835G>A (p.Asp279Asn) rs368796800 0.00001
NM_002880.4(RAF1):c.93A>G (p.Thr31=) rs762478810 0.00001
NM_002880.4(RAF1):c.990+9A>G rs559532794 0.00001
NM_002880.3(RAF1):c.-340_-339GA[1] rs527774250
NM_002880.4(RAF1):c.-204G>C rs547543588
NM_002880.4(RAF1):c.-267G>A rs116247741
NM_002880.4(RAF1):c.-27+8G>T rs1553626725
NM_002880.4(RAF1):c.-298C>T rs727504387
NM_002880.4(RAF1):c.-34T>C rs1553626734
NM_002880.4(RAF1):c.1108+9_1108+21del rs727504451
NM_002880.4(RAF1):c.1314C>T (p.Thr438=) rs147547744
NM_002880.4(RAF1):c.1356G>A (p.Thr452=) rs766112769
NM_002880.4(RAF1):c.1537-19C>T
NM_002880.4(RAF1):c.1629G>T (p.Thr543=) rs5746244
NM_002880.4(RAF1):c.1668+19G>A rs5746245
NM_002880.4(RAF1):c.168C>T (p.Asn56=) rs1553616614
NM_002880.4(RAF1):c.1695T>C (p.Tyr565=) rs397516817
NM_002880.4(RAF1):c.1803+6G>C rs1553609870
NM_002880.4(RAF1):c.21T>C (p.Ala7=) rs886057915
NM_002880.4(RAF1):c.231C>T (p.Ser77=) rs1450510914
NM_002880.4(RAF1):c.276A>G (p.Gln92=) rs876657568
NM_002880.4(RAF1):c.320+17C>A rs897042666
NM_002880.4(RAF1):c.534C>T (p.Thr178=) rs1553614692
NM_002880.4(RAF1):c.606T>C (p.Gly202=) rs754197477
NM_002880.4(RAF1):c.678T>G (p.Val226=) rs1553614183
NM_002880.4(RAF1):c.680+11A>G rs868108376
NM_002880.4(RAF1):c.834+8G>A rs727504615
NM_002880.4(RAF1):c.835-20G>C rs745899008
NM_002880.4(RAF1):c.876C>T (p.Ala292=) rs397516831
NM_002880.4(RAF1):c.981A>G (p.Lys327=) rs2058814646

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