Colon Cancer: Gene >> PSMD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000210313
Start	120817931:120817931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752722111
CDS Mutation	c.1490C>T
AA Mutation	p.Thr497Met(p.T497M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000210313
Start	120831447:120831447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.445C>A
AA Mutation	p.Leu149Met(p.L149M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000210313
Start	120831853:120831853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.411G>T
AA Mutation	p.Glu137Asp(p.E137D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000210313
Start	120826784:120826784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000210313
Start	120833336:120833336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.294T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000210313
Start	120824668:120824669(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.831dupT
AA Mutation	p.Gly278TrpfsTer8(p.G278Wfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000210313
Start	120818013:120818014(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1407_1408insCTA
AA Mutation	p.Ile469_Ala470insLeu(p.I469_A470insL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PSMD5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000210313
Start	120826834:120826834(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.745G>T
AA Mutation	p.Val249Leu(p.V249L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript