Colon Cancer: Gene >> CYBB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37804097:37804097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1118A>G
AA Mutation	p.Lys373Arg(p.K373R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37806432:37806432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1360T>C
AA Mutation	p.Phe454Leu(p.F454L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37793797:37793797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781797749
CDS Mutation	c.470G>A
AA Mutation	p.Arg157Gln(p.R157Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37796090:37796090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.623C>T
AA Mutation	p.Thr208Ile(p.T208I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378588
Start	37783566:37783566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.218G>A
AA Mutation	p.Arg73Gln(p.R73Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378588
Start	37796079:37796079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.612C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378588
Start	37805012:37805012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374511592
CDS Mutation	c.1158G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378588
Start	37796043:37796043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.576C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000378588
Start	37801319:37801319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.868C>T
AA Mutation	p.Arg290Ter(p.R290*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYBB

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000378588
Start	37791993:37791993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript