Colon Cancer: Gene >> ENTPD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371205
Start	95866345:95866345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1495T>G
AA Mutation	p.Phe499Val(p.F499V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371205
Start	95842450:95842450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.369G>T
AA Mutation	p.Glu123Asp(p.E123D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371205
Start	95864826:95864826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1291G>A
AA Mutation	p.Ala431Thr(p.A431T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371205
Start	95845392:95845392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371205
Start	95823244:95823244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368856010
CDS Mutation	c.24C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371205
Start	95839774:95839774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538046581
CDS Mutation	c.228C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371205
Start	95844558:95844573(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.500_515delGGATCATTACTGGCCA
AA Mutation	p.Arg167LysfsTer27(p.R167Kfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000371205
Start	95844489:95844489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.427G>T
AA Mutation	p.Glu143Ter(p.E143*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ENTPD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371205
Start	95845564:95845564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781G>A
AA Mutation	p.Ala261Thr(p.A261T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript