Colon Cancer: Gene >> MYCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897424:39897424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775863077
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897595:39897595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748297163
CDS Mutation	c.872G>A
AA Mutation	p.Arg291His(p.R291H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897862:39897862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605A>G
AA Mutation	p.His202Arg(p.H202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897734:39897734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.733G>A
AA Mutation	p.Glu245Lys(p.E245K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897389:39897389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1078T>C
AA Mutation	p.Tyr360His(p.Y360H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897719:39897719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.748G>A
AA Mutation	p.Glu250Lys(p.E250K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000372816
Start	39901315:39901315(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.120delC
AA Mutation	p.Thr41ArgfsTer69(p.T41Rfs*69)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000372816
Start	39897893:39897893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.574C>T
AA Mutation	p.Arg192Ter(p.R192*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MYCL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897628:39897628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839T>A
AA Mutation	p.Val280Glu(p.V280E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000372816
Start	39897694:39897694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>A
AA Mutation	p.Pro258Gln(p.P258Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript