Colon Cancer: Gene >> ADK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286621
Start	74600446:74600446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562751709
CDS Mutation	c.830G>A
AA Mutation	p.Arg277Gln(p.R277Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286621
Start	74314698:74314698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.226G>A
AA Mutation	p.Glu76Lys(p.E76K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286621
Start	74151322:74151322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.44T>C
AA Mutation	p.Val15Ala(p.V15A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286621
Start	74525259:74525259(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs771117099
CDS Mutation	c.564delT
AA Mutation	p.Thr190GlnfsTer8(p.T190Qfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286621
Start	74398554:74398554(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.534delA
AA Mutation	p.Ala179GlnfsTer6(p.A179Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000286621
Start	74600394:74600394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.778G>T
AA Mutation	p.Glu260Ter(p.E260*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ADK

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286621
Start	74394209:74394209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286621
Start	74314697:74314697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780042061
CDS Mutation	c.225C>T
Mutation Classification	Silent
Feature Type	Transcript