Colon Cancer: Gene >> NPEPPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322157
Start	47585504:47585504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.653T>C
AA Mutation	p.Val218Ala(p.V218A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322157
Start	47579485:47579485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514C>T
AA Mutation	p.Arg172Cys(p.R172C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322157
Start	47596358:47596358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1432C>A
AA Mutation	p.Leu478Ile(p.L478I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322157
Start	47619043:47619043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2438T>C
AA Mutation	p.Ile813Thr(p.I813T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322157
Start	47531453:47531453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000322157
Start	47587254:47587254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1010delA
AA Mutation	p.Asn337IlefsTer37(p.N337Ifs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000322157
Start	47618371:47618371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2317C>T
AA Mutation	p.Gln773Ter(p.Q773*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000322157
Start	47531376:47531378(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.78_80delTCT
AA Mutation	p.Leu27del(p.L27del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NPEPPS

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322157
Start	47582826:47582826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Asp209Asn(p.D209N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript