ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 58
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_004333.6(BRAF):c.-19C>T rs71645935 0.01115
NM_004333.6(BRAF):c.1433-19A>G rs369635503 0.00114
NM_004333.6(BRAF):c.2127+3A>G rs371976102 0.00043
NM_004333.6(BRAF):c.-5A>G rs71645936 0.00024
NM_004333.6(BRAF):c.483G>C (p.Leu161=) rs61730029 0.00016
NM_004333.6(BRAF):c.1141-12A>G rs375704079 0.00014
NM_004333.6(BRAF):c.504+17A>G rs201797624 0.00013
NM_004333.6(BRAF):c.1632T>C (p.Ile544=) rs149702741 0.00010
NM_004333.6(BRAF):c.375T>G (p.Ser125=) rs201507202 0.00008
NM_004333.6(BRAF):c.1433-5T>C rs587780861 0.00006
NM_004333.6(BRAF):c.504+19C>T rs780617193 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.1667T>C (p.Ile556Thr) rs760524720 0.00004
NM_004333.6(BRAF):c.1694+14G>A rs184144181 0.00003
NM_004333.6(BRAF):c.2136C>T (p.Ala712=) rs377165711 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.*7T>C rs727502903 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.1236C>T (p.Asn412=) rs397516888 0.00001
NM_004333.6(BRAF):c.1314+12T>C rs765090629 0.00001
NM_004333.6(BRAF):c.1347T>C (p.Asp449=) rs397516889 0.00001
NM_004333.6(BRAF):c.193T>C (p.Leu65=) rs866875749 0.00001
NM_004333.6(BRAF):c.2082A>G (p.Ala694=) rs375174370 0.00001
NM_004333.6(BRAF):c.2128-10T>C rs397516898 0.00001
NM_004333.6(BRAF):c.2229T>C (p.Phe743=) rs397516901 0.00001
NM_004333.6(BRAF):c.439A>G (p.Ser147Gly) rs397507464 0.00001
NM_004333.6(BRAF):c.675A>G (p.Glu225=) rs755993280 0.00001
NM_004333.6(BRAF):c.714A>T (p.Val238=) rs397516902 0.00001
NM_004333.6(BRAF):c.73C>T (p.Pro25Ser) rs730880412 0.00001
NM_004333.6(BRAF):c.750T>C (p.Phe250=) rs754568893 0.00001
NM_001378469.1(BRAF):c.1178-35T>C rs397516887
NM_004333.6(BRAF):c.111G>A (p.Ser37=) rs727502906
NM_004333.6(BRAF):c.1203C>T (p.Thr401=) rs370130654
NM_004333.6(BRAF):c.1206C>T (p.Pro402=) rs201758035
NM_004333.6(BRAF):c.1207C>G (p.Pro403Ala) rs749792302
NM_004333.6(BRAF):c.1245C>T (p.Ala415=)
NM_004333.6(BRAF):c.1956A>C (p.Gly652=) rs1554392528
NM_004333.6(BRAF):c.1960T>C (p.Leu654=) rs727502905
NM_004333.6(BRAF):c.1993-11dup rs759069424
NM_004333.6(BRAF):c.2064C>T (p.Ala688=) rs1554389847
NM_004333.6(BRAF):c.2128-16_2128-15delinsTC rs2130870208
NM_004333.6(BRAF):c.2128-5del rs373442098
NM_004333.6(BRAF):c.2128-6T>A rs397516900
NM_004333.6(BRAF):c.213G>A (p.Glu71=)
NM_004333.6(BRAF):c.2224G>A (p.Asp742Asn) rs1057520665
NM_004333.6(BRAF):c.241-8T>A rs963659807
NM_004333.6(BRAF):c.279A>G (p.Gln93=) rs150050723
NM_004333.6(BRAF):c.612G>A (p.Glu204=) rs1202874043
NM_004333.6(BRAF):c.669T>C (p.His223=) rs2129047893
NM_004333.6(BRAF):c.711+15A>G rs1554404457
NM_004333.6(BRAF):c.76G>A (p.Glu26Lys) rs397507457
NM_004333.6(BRAF):c.83GCGCCG[2] (p.28GA[2]) rs397507458
NM_004333.6(BRAF):c.83GCGCCG[4] (p.28GA[4]) rs397507458
NM_004333.6(BRAF):c.855A>G (p.Gln285=) rs376575252
NM_004333.6(BRAF):c.918C>G (p.Ser306=) rs794727865

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.