Colon Cancer: Gene >> PPID

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307720
Start	158715376:158715376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.673G>A
AA Mutation	p.Asp225Asn(p.D225N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307720
Start	158710827:158710827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916A>C
AA Mutation	p.Asn306His(p.N306H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000307720
Start	158719227:158719227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>T
AA Mutation	p.Glu96Ter(p.E96*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307720
Start	158717134:158717135(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.399dupT
AA Mutation	p.Ile134TyrfsTer21(p.I134Yfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> PPID

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307720
Start	158715395:158715395(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654A>C
AA Mutation	p.Lys218Asn(p.K218N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307720
Start	158719248:158719248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265A>C
AA Mutation	p.Asn89His(p.N89H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000307720
Start	158710779:158710779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.964G>T
AA Mutation	p.Glu322Ter(p.E322*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript