ClinVar Miner

List of variants in gene BRAF reported as likely benign by GeneDx

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Gene type:
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Total variants: 79
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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.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.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.1178-271T>C rs189649654 0.00292
NM_004333.6(BRAF):c.2127+206A>G rs71645991 0.00108
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.1632T>C (p.Ile544=) rs149702741 0.00010
NM_004333.6(BRAF):c.1993-11T>C rs750297886 0.00009
NM_004333.6(BRAF):c.1694+13C>T rs368578780 0.00007
NM_004333.6(BRAF):c.504+19C>T rs780617193 0.00006
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.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.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.1518-7T>C rs199745091 0.00002
NM_004333.6(BRAF):c.240+6C>T rs1320075163 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.1314+12T>C rs765090629 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.439A>G (p.Ser147Gly) rs397507464 0.00001
NM_004333.6(BRAF):c.567T>C (p.Gly189=) rs1057523903 0.00001
NM_004333.6(BRAF):c.675A>G (p.Glu225=) rs755993280 0.00001
NM_004333.6(BRAF):c.73C>T (p.Pro25Ser) rs730880412 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.969G>A (p.Ser323=) rs768134774 0.00001
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.1177+224_1177+225dup rs1199383417
NM_004333.6(BRAF):c.1177+247del rs1199383417
NM_004333.6(BRAF):c.1206C>A (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1368G>A (p.Gln456=) rs767473452
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.1956A>C (p.Gly652=) rs1554392528
NM_004333.6(BRAF):c.1993-11dup rs759069424
NM_004333.6(BRAF):c.2127+282dup rs11360482
NM_004333.6(BRAF):c.2128-27_2128-18del rs774138098
NM_004333.6(BRAF):c.2224G>A (p.Asp742Asn) rs1057520665
NM_004333.6(BRAF):c.241-8T>A rs963659807
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.711+15A>G rs1554404457
NM_004333.6(BRAF):c.76G>A (p.Glu26Lys) rs397507457
NM_004333.6(BRAF):c.855A>G (p.Gln285=) rs376575252
NM_004333.6(BRAF):c.876C>T (p.Ser292=) rs1554403310

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