Colon Cancer: Gene >> IRF4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000380956
Start	393255:393255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.103G>A
AA Mutation	p.Gly35Ser(p.G35S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000380956
Start	401645:401645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967G>A
AA Mutation	p.Gly323Arg(p.G323R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000380956
Start	401682:401682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1004A>C
AA Mutation	p.Tyr335Ser(p.Y335S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000380956
Start	407546:407546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1304G>A
AA Mutation	p.Ser435Asn(p.S435N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000380956
Start	397219:397219(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143144957
CDS Mutation	c.604G>A
AA Mutation	p.Gly202Ser(p.G202S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380956
Start	401668:401668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380956
Start	395911:395911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765193356
CDS Mutation	c.468G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380956
Start	398901:398901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380956
Start	401482:401482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769596072
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000380956
Start	407568:407568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1326A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> IRF4

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000380956
Start	407593:407593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1351G>T
AA Mutation	p.Glu451Ter(p.E451*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript