BrainBase
a curated knowledgebase for brain diseases
Sample ID |
Gene Symbol |
Glioma Grade |
Chr |
Start Site |
End Site |
RET |
ALT |
Amino Acid Change |
Effect |
Filter |
DNA VAF |
TCGA-TM-A7C3-01A |
PRAMEF18 |
LGG |
chr1 |
13225205 |
13225205 |
C |
A |
p.Q174H |
missense_variant |
PASS |
0.116040956 |
TCGA-TM-A7C3-01A |
MKNK1 |
LGG |
chr1 |
46558727 |
46558727 |
C |
T |
p.E416K |
missense_variant |
PASS |
0.153846154 |
TCGA-TM-A7C3-01A |
FGFR1 |
LGG |
chr1 |
152308926 |
152308926 |
C |
T |
p.R1987H |
missense_variant |
PASS |
0.421686747 |
TCGA-TM-A7C3-01A |
EFNA3 |
LGG |
chr1 |
155086158 |
155086158 |
C |
T |
p.T180I |
missense_variant |
PASS |
0.269230769 |
TCGA-TM-A7C3-01A |
ARHGEF2 |
LGG |
chr1 |
155965742 |
155965742 |
G |
A |
p.P120L |
missense_variant |
PASS |
0.295454545 |
TCGA-TM-A7C3-01A |
SOAT1 |
LGG |
chr1 |
179350306 |
179350306 |
A |
G |
p.K442R |
missense_variant |
PASS |
0.411764706 |
TCGA-TM-A7C3-01A |
USH2A |
LGG |
chr1 |
215634664 |
215634664 |
C |
T |
p.R5031Q |
missense_variant |
PASS |
0.344086022 |
TCGA-TM-A7C3-01A |
OR2T4 |
LGG |
chr1 |
248362393 |
248362393 |
C |
A |
p.A271A |
synonymous_variant |
PASS |
0.433333333 |
TCGA-TM-A7C3-01A |
CPSF3 |
LGG |
chr2 |
9433898 |
9433898 |
C |
A |
p.Q183K |
missense_variant |
PASS |
0.385714286 |
TCGA-TM-A7C3-01A |
SCN3A |
LGG |
chr2 |
165140656 |
165140656 |
G |
A |
p.P672S |
missense_variant |
PASS |
0.457627119 |