Table 2 Consistent mutations shared with the sample from TCGA database
Gene | Position | Transcript ID | Exon | Coding sequence change | Protein change | Variant type | Cancer type |
|---|---|---|---|---|---|---|---|
DNMT3A | chr2:25523009 | NM_022552 | 3 | c.176delC | p.P59fs | frameshift deletion | STAD, UCEC |
PIK3CB | chr3:138413710 | NM_001256045 | 3 | c.346delC | p.R116fs | frameshift deletion | UCEC |
FGFR3 | chr4:1807545 | NM_022965 | 11 | c.1378delC | p.P460fs | frameshift deletion | STAD |
BRD3 | chr9:136918529 | NM_007371 | 2 | c.71delC | p.P24fs | frameshift deletion | COAD |
BRCA2 | chr13:32913428 | NM_000059 | 11 | c.4936G > C | p.E1646Q | missense | LUAD |
PSMB5 | chr14:23502760 | NM_001130725 | 2 | c.G13A | p.A5T | missense | PAAD |
NOTCH3 | chr19:15296358 | NM_000435 | 13 | c.2084delC | p.P695fs | frameshift deletion | STAD, UCEC |
GNAS | chr20:57415178 | NM_016592 | 1 | c.G17A | p.R6Q | missense | HNSC |
BCR | chr22:23654017 | NM_021574 | 18 | c.G3184A | p.D1062N | missense | STAD |