ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 142
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.1517+185G>A rs117044637 0.01860
NM_004333.6(BRAF):c.861-170A>T rs3748093 0.01557
NM_004333.6(BRAF):c.78G>T (p.Glu26Asp) rs371877084 0.01088
NM_004333.6(BRAF):c.1178-104C>G rs71645967 0.00976
NM_004333.4(BRAF):c.-295G>A rs71645931 0.00868
NM_004333.6(BRAF):c.505-292G>A rs111570437 0.00842
NM_004333.6(BRAF):c.1315-338C>T rs6952069 0.00839
NM_004333.6(BRAF):c.2128-210A>G rs71645994 0.00795
NM_004333.6(BRAF):c.1518-117A>T rs71645984 0.00740
NC_000007.14:g.140924965G>A rs71645932 0.00733
NM_004333.6(BRAF):c.504+76A>G rs71645948 0.00708
NM_004333.6(BRAF):c.138+226C>G rs71645938 0.00707
NM_004333.6(BRAF):c.240+72A>G rs71645941 0.00460
NM_004333.6(BRAF):c.1141-110G>A rs117001169 0.00440
NM_004333.6(BRAF):c.1177+1073C>T rs147309367 0.00385
NM_004333.6(BRAF):c.2128-280T>C rs61646556 0.00385
NM_004333.6(BRAF):c.1860+156T>A rs71645989 0.00363
NM_004333.6(BRAF):c.1433-162T>G rs71645978 0.00362
NM_004333.6(BRAF):c.241-149A>G rs71645946 0.00362
NM_004333.6(BRAF):c.1177+158C>T rs71645961 0.00360
NM_004333.6(BRAF):c.1314+153G>C rs71645968 0.00360
NM_004333.6(BRAF):c.1227A>G (p.Ser409=) rs145035762 0.00318
NM_004333.6(BRAF):c.1178-271T>C rs189649654 0.00292
NM_004333.6(BRAF):c.1140+2523G>C rs190814468 0.00278
NM_004333.6(BRAF):c.1433-19A>G rs369635503 0.00114
NM_004333.6(BRAF):c.2127+206A>G rs71645991 0.00108
NM_004333.6(BRAF):c.1332G>A (p.Arg444=) rs56101602 0.00068
NM_004333.6(BRAF):c.980+1812C>T rs1046366661 0.00030
NM_004333.6(BRAF):c.64G>A (p.Asp22Asn) rs397507456 0.00025
NM_004333.6(BRAF):c.1742-29A>G rs143181039 0.00019
NM_004333.6(BRAF):c.1860+16A>G rs368859030 0.00016
NM_004333.6(BRAF):c.1141-12A>G rs375704079 0.00014
NM_004333.6(BRAF):c.723G>A (p.Thr241=) rs369182143 0.00013
NM_004333.6(BRAF):c.36G>A (p.Ala12=) rs397507454 0.00011
NM_004333.6(BRAF):c.1632T>C (p.Ile544=) rs149702741 0.00010
NM_004333.6(BRAF):c.1993-11T>C rs750297886 0.00009
NM_004333.6(BRAF):c.375T>G (p.Ser125=) rs201507202 0.00008
NM_004333.6(BRAF):c.1694+13C>T rs368578780 0.00007
NM_004333.6(BRAF):c.505-12A>G rs377433501 0.00006
NM_004333.6(BRAF):c.52C>G (p.Leu18Val) rs1222192591 0.00006
NM_004333.6(BRAF):c.92C>G (p.Ala31Gly) rs397516906 0.00006
NM_004333.6(BRAF):c.2196C>G (p.Ser732=) rs142592480 0.00005
NM_004333.6(BRAF):c.72G>C (p.Glu24Asp) rs587778114 0.00005
NM_004333.6(BRAF):c.915G>A (p.Ala305=) rs145675911 0.00004
NM_004333.6(BRAF):c.1314+17T>C rs1057524397 0.00003
NM_004333.6(BRAF):c.2128-15T>C rs763538892 0.00003
NM_004333.6(BRAF):c.622A>G (p.Ile208Val) rs727504571 0.00003
NM_004333.6(BRAF):c.708C>T (p.Asn236=) rs138333692 0.00003
NM_004333.6(BRAF):c.861T>C (p.Asp287=) rs761326211 0.00003
NM_004333.6(BRAF):c.1144T>A (p.Leu382Met) rs147732750 0.00002
NM_004333.6(BRAF):c.1315-28A>G rs776147874 0.00002
NM_004333.6(BRAF):c.138+17C>G rs756400234 0.00002
NM_004333.6(BRAF):c.240+6C>T rs1320075163 0.00002
NM_004333.6(BRAF):c.357C>T (p.Thr119=) rs552456345 0.00002
NM_004333.6(BRAF):c.-24dup rs1395865715 0.00001
NM_004333.6(BRAF):c.1236C>T (p.Asn412=) rs397516888 0.00001
NM_004333.6(BRAF):c.1305G>A (p.Arg435=) rs763771673 0.00001
NM_004333.6(BRAF):c.1818G>A (p.Gly606=) rs1797931923 0.00001
NM_004333.6(BRAF):c.259A>G (p.Ser87Gly) rs876661018 0.00001
NM_004333.6(BRAF):c.437G>A (p.Arg146Gln) rs557241012 0.00001
NM_004333.6(BRAF):c.567T>C (p.Gly189=) rs1057523903 0.00001
NM_004333.6(BRAF):c.81C>G (p.Ala27=) rs1330565982 0.00001
NM_004333.6(BRAF):c.901C>T (p.Pro301Ser) rs34776339 0.00001
NM_004333.6(BRAF):c.951C>A (p.Ser317=) rs755298519 0.00001
NM_004333.6(BRAF):c.969G>A (p.Ser323=) rs768134774 0.00001
NC_000007.14:g.140798273_140798276T[4]CTTTTTTTTTTT[1]
NC_000007.14:g.140798273_140798279T[7]CTTTTTTTTTTT[1]
NM_001374258.1(BRAF):c.*124C>T
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.1140+2154G>T
NM_004333.6(BRAF):c.1140+2157A>G
NM_004333.6(BRAF):c.1140+2236T>C
NM_004333.6(BRAF):c.1140+2553_1140+2554del
NM_004333.6(BRAF):c.1140+2738G>A
NM_004333.6(BRAF):c.1140+3283G>A
NM_004333.6(BRAF):c.1140+3314C>T
NM_004333.6(BRAF):c.1140+804_1140+805insTA
NM_004333.6(BRAF):c.1140+815A>G
NM_004333.6(BRAF):c.1141-1355C>T
NM_004333.6(BRAF):c.1141-137T>C
NM_004333.6(BRAF):c.1141-1927C>T
NM_004333.6(BRAF):c.1141-1946G>A
NM_004333.6(BRAF):c.1141-2272C>T
NM_004333.6(BRAF):c.1141-3287G>A
NM_004333.6(BRAF):c.1141-370C>T
NM_004333.6(BRAF):c.1141-529G>T
NM_004333.6(BRAF):c.1141-563A>T
NM_004333.6(BRAF):c.1141-58C>T
NM_004333.6(BRAF):c.1141-632A>G
NM_004333.6(BRAF):c.1177+1386G>A
NM_004333.6(BRAF):c.1177+1621C>T
NM_004333.6(BRAF):c.1177+2192T>G
NM_004333.6(BRAF):c.1177+224_1177+225dup rs1199383417
NM_004333.6(BRAF):c.1177+245_1177+247dup rs1199383417
NM_004333.6(BRAF):c.1177+247del rs1199383417
NM_004333.6(BRAF):c.1178-1093G>T
NM_004333.6(BRAF):c.1178-1184C>T
NM_004333.6(BRAF):c.1178-1954dup
NM_004333.6(BRAF):c.1178-860T>G
NM_004333.6(BRAF):c.1178-946_1178-943dup
NM_004333.6(BRAF):c.1206C>A (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1278G>A (p.Arg426=) rs1586146368
NM_004333.6(BRAF):c.1315-105C>G
NM_004333.6(BRAF):c.1315-131T>C
NM_004333.6(BRAF):c.1315-407A>G
NM_004333.6(BRAF):c.1368G>A (p.Gln456=) rs767473452
NM_004333.6(BRAF):c.138+80G>A
NM_004333.6(BRAF):c.141G>A (p.Val47=) rs2129073776
NM_004333.6(BRAF):c.1433-7C>G rs1057522055
NM_004333.6(BRAF):c.1518-117dup rs925184421
NM_004333.6(BRAF):c.1518-282T>G rs71645982
NM_004333.6(BRAF):c.1518-5T>C rs940384157
NM_004333.6(BRAF):c.156A>G (p.Gln52=) rs1190976562
NM_004333.6(BRAF):c.1694+8C>T rs1057520453
NM_004333.6(BRAF):c.1742-10T>G rs730880411
NM_004333.6(BRAF):c.1993-11dup rs759069424
NM_004333.6(BRAF):c.2127+282dup rs11360482
NM_004333.6(BRAF):c.2128-16_2128-7del rs766844227
NM_004333.6(BRAF):c.2128-27_2128-18del rs774138098
NM_004333.6(BRAF):c.2128-5dup rs373442098
NM_004333.6(BRAF):c.288A>G (p.Glu96=)
NM_004333.6(BRAF):c.342T>C (p.Ser114=)
NM_004333.6(BRAF):c.608+19G>C rs200908826
NM_004333.6(BRAF):c.609-294_609-290del rs35843886
NM_004333.6(BRAF):c.609-315_609-313dup rs35843886
NM_004333.6(BRAF):c.609-315dup rs35843886
NM_004333.6(BRAF):c.687T>C (p.Asn229=) rs1586237175
NM_004333.6(BRAF):c.862T>C (p.Leu288=) rs773839216
NM_004333.6(BRAF):c.876C>T (p.Ser292=) rs1554403310
NM_004333.6(BRAF):c.980+1221G>A
NM_004333.6(BRAF):c.980+1615C>T
NM_004333.6(BRAF):c.980+1809del
NM_004333.6(BRAF):c.980+2510T>A
NM_004333.6(BRAF):c.980+2726G>T
NM_004333.6(BRAF):c.980+2809G>A
NM_004333.6(BRAF):c.980+483C>A
NM_004333.6(BRAF):c.980+601T>C
NM_004333.6(BRAF):c.980+812T>C
NM_004333.6(BRAF):c.981-1264A>G
NM_004333.6(BRAF):c.981-1315dup
NM_004333.6(BRAF):c.981-2805G>C
NM_004333.6(BRAF):c.981-2908A>G

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.