Colon Cancer: Gene >> IRAK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369980
Start	154019454:154019454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369980
Start	154012673:154012673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1936G>A
AA Mutation	p.Ala646Thr(p.A646T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369980
Start	154016532:154016532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1141A>T
AA Mutation	p.Thr381Ser(p.T381S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369980
Start	154019002:154019002(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.513G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369980
Start	154013347:154013347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150089165
CDS Mutation	c.1626G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369980
Start	154018653:154018653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.675C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369980
Start	154013354:154013354(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1619delC
AA Mutation	p.Pro540LeufsTer53(p.P540Lfs*53)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IRAK1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369980
Start	154011862:154011862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2136C>T
Mutation Classification	Silent
Feature Type	Transcript