ClinVar Miner

List of variants in gene RAF1 studied for not specified

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Total variants: 164
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HGVS dbSNP gnomAD frequency
NM_002880.4(RAF1):c.1669-36C>T rs3729931 0.43953
NM_002880.4(RAF1):c.1755A>G (p.Val585=) rs3730296 0.02125
NM_002880.4(RAF1):c.1193+39T>C rs2290161 0.01394
NM_002880.3(RAF1):c.-415-1C>G rs61730434 0.01127
NM_002880.4(RAF1):c.-281C>G rs61761285 0.01090
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.1669-13T>C rs147475396 0.00819
NM_002880.4(RAF1):c.923C>T (p.Pro308Leu) rs5746220 0.00571
NM_002880.4(RAF1):c.208-17T>C rs3730268 0.00529
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.-201C>A rs532668125 0.00073
NM_002880.4(RAF1):c.-209G>A rs727504351 0.00035
NM_002880.4(RAF1):c.-59C>A rs201603517 0.00032
NM_002880.4(RAF1):c.321-14T>A rs3730270 0.00032
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.1537-11G>A rs182394722 0.00024
NM_002880.4(RAF1):c.119G>A (p.Arg40His) rs192632236 0.00016
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.1587G>A (p.Ser529=) rs114687276 0.00014
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.1537-13G>A rs369039413 0.00011
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.1107C>T (p.His369=) rs761947194 0.00006
NM_002880.4(RAF1):c.1371-15C>A rs371491379 0.00006
NM_002880.4(RAF1):c.1814C>T (p.Ser605Phe) rs730881004 0.00006
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.1663G>C (p.Asp555His) rs371704292 0.00004
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.570C>T (p.Ile190=) rs780912024 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.1109-17G>C rs770431112 0.00003
NM_002880.4(RAF1):c.1821G>A (p.Glu607=) rs747437834 0.00003
NM_002880.4(RAF1):c.1921A>G (p.Thr641Ala) rs1183812590 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_002880.3(RAF1):c.-361G>T rs727504376 0.00002
NM_002880.4(RAF1):c.1193+17C>T rs753928357 0.00002
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.1668+4A>G rs771344560 0.00002
NM_002880.4(RAF1):c.1669-14T>C rs1260935888 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.819C>G (p.Asp273Glu) rs771675427 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_002880.4(RAF1):c.952C>T (p.Arg318Trp) rs759433668 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.-4A>C rs368465923 0.00001
NM_002880.4(RAF1):c.1063A>G (p.Ile355Val) rs727504719 0.00001
NM_002880.4(RAF1):c.1141G>A (p.Asp381Asn) rs559632360 0.00001
NM_002880.4(RAF1):c.1193+18G>C rs201845942 0.00001
NM_002880.4(RAF1):c.1247A>G (p.Asn416Ser) rs774198365 0.00001
NM_002880.4(RAF1):c.1334T>G (p.Leu445Arg) rs757591797 0.00001
NM_002880.4(RAF1):c.1355C>T (p.Thr452Met) rs555781462 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.1688G>A (p.Arg563Gln) rs727504827 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.1741A>G (p.Met581Val) rs752063874 0.00001
NM_002880.4(RAF1):c.1895_1918del (p.Glu632_Thr640delinsAla) rs2058255431 0.00001
NM_002880.4(RAF1):c.1910G>A (p.Cys637Tyr) rs769639669 0.00001
NM_002880.4(RAF1):c.1914G>A (p.Thr638=) rs144876026 0.00001
NM_002880.4(RAF1):c.1928C>T (p.Pro643Leu) rs1382398408 0.00001
NM_002880.4(RAF1):c.321T>C (p.Gly107=) rs201937982 0.00001
NM_002880.4(RAF1):c.331C>T (p.Arg111Cys) rs773801570 0.00001
NM_002880.4(RAF1):c.391C>T (p.Leu131=) rs878854566 0.00001
NM_002880.4(RAF1):c.424-6T>C rs983999914 0.00001
NM_002880.4(RAF1):c.471A>G (p.Lys157=) rs1001494773 0.00001
NM_002880.4(RAF1):c.482A>G (p.Asn161Ser) rs775781057 0.00001
NM_002880.4(RAF1):c.536A>G (p.Lys179Arg) rs1271531726 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.845G>A (p.Arg282Gln) rs752713997 0.00001
NM_002880.4(RAF1):c.93A>G (p.Thr31=) rs762478810 0.00001
NM_002880.4(RAF1):c.974A>C (p.Gln325Pro) rs764719098 0.00001
NM_002880.4(RAF1):c.990+9A>G rs559532794 0.00001
NM_002880.3(RAF1):c.(?_-26)-50_(1370_?)+72dup
NM_002880.3(RAF1):c.-340_-339GA[1] rs527774250
NM_002880.3(RAF1):c.1804-11_1804-7dup rs727503382
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.-40C>T rs727503385
NM_002880.4(RAF1):c.1016G>A (p.Ser339Asn) rs1057518084
NM_002880.4(RAF1):c.1108+9_1108+21del rs727504451
NM_002880.4(RAF1):c.1144C>T (p.Pro382Ser) rs1575546471
NM_002880.4(RAF1):c.1193+13C>T
NM_002880.4(RAF1):c.1194-17TCCCC[2] rs2058496555
NM_002880.4(RAF1):c.124_125delinsAT (p.Ala42Ile) rs876657965
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.1483C>T (p.Arg495Cys)
NM_002880.4(RAF1):c.1528C>T (p.Leu510Phe) rs397516816
NM_002880.4(RAF1):c.1537-19C>T
NM_002880.4(RAF1):c.1613T>C (p.Leu538Ser) rs730881011
NM_002880.4(RAF1):c.1629G>T (p.Thr543=) rs5746244
NM_002880.4(RAF1):c.1668+10_1668+11del rs730880997
NM_002880.4(RAF1):c.1668+19G>A rs5746245
NM_002880.4(RAF1):c.1668+19G>T rs5746245
NM_002880.4(RAF1):c.1673T>C (p.Ile558Thr) rs1559399152
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.1708C>G (p.Leu570Val) rs876657966
NM_002880.4(RAF1):c.1720_1760dup (p.Asp587_Cys588insIleArgThrAlaProLysGlnTer) rs2058275378
NM_002880.4(RAF1):c.1724A>C (p.Lys575Thr) rs767890715
NM_002880.4(RAF1):c.172A>C (p.Ile58Leu) rs147984543
NM_002880.4(RAF1):c.1770G>C (p.Lys590Asn) rs773583951
NM_002880.4(RAF1):c.1803+6G>C rs1553609870
NM_002880.4(RAF1):c.1842G>A (p.Pro614=) rs200235582
NM_002880.4(RAF1):c.1927C>T (p.Pro643Ser) rs876657967
NM_002880.4(RAF1):c.207+10C>T rs2059446210
NM_002880.4(RAF1):c.21T>C (p.Ala7=) rs886057915
NM_002880.4(RAF1):c.226A>G (p.Met76Val) rs730880999
NM_002880.4(RAF1):c.231C>T (p.Ser77=) rs1450510914
NM_002880.4(RAF1):c.237T>G (p.His79Gln) rs876661384
NM_002880.4(RAF1):c.276A>G (p.Gln92=) rs876657568
NM_002880.4(RAF1):c.320+17C>A rs897042666
NM_002880.4(RAF1):c.321-14dup rs202103447
NM_002880.4(RAF1):c.321-4delinsTG rs2125421173
NM_002880.4(RAF1):c.325_327del (p.Lys109del) rs1418886913
NM_002880.4(RAF1):c.329C>T (p.Ala110Val) rs397516819
NM_002880.4(RAF1):c.379C>G (p.Gln127Glu) rs397516820
NM_002880.4(RAF1):c.388T>A (p.Phe130Ile) rs397516821
NM_002880.4(RAF1):c.419A>G (p.Asn140Ser) rs876657968
NM_002880.4(RAF1):c.424G>T (p.Ala142Ser) rs1553614748
NM_002880.4(RAF1):c.512A>G (p.Lys171Arg) rs876657969
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.68_70del (p.Asp23del) rs749549707
NM_002880.4(RAF1):c.752T>A (p.Leu251His) rs1553613787
NM_002880.4(RAF1):c.775T>G (p.Ser259Ala) rs3730271
NM_002880.4(RAF1):c.776C>A (p.Ser259Tyr) rs397516827
NM_002880.4(RAF1):c.784A>C (p.Asn262His) rs1575573204
NM_002880.4(RAF1):c.834+8G>A rs727504615
NM_002880.4(RAF1):c.835-20G>C rs745899008
NM_002880.4(RAF1):c.837T>A (p.Asp279Glu) rs2125381916
NM_002880.4(RAF1):c.856G>A (p.Glu286Lys) rs147453956
NM_002880.4(RAF1):c.876C>T (p.Ala292=) rs397516831
NM_002880.4(RAF1):c.981A>G (p.Lys327=) rs2058814646
NM_002880.4(RAF1):c.991-17A>G
Single allele

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