Colon Cancer: Gene >> PISD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31619745:31619745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567105342
CDS Mutation	c.1097G>A
AA Mutation	p.Arg366His(p.R366H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31650705:31650705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760491476
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31648228:31648228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373015840
CDS Mutation	c.194G>A
AA Mutation	p.Arg65His(p.R65H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31621139:31621139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760199435
CDS Mutation	c.701C>T
AA Mutation	p.Ala234Val(p.A234V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000439502
Start	31621682:31621682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368409664
CDS Mutation	c.525G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PISD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31620648:31620648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370672474
CDS Mutation	c.910C>T
AA Mutation	p.Arg304Trp(p.R304W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000439502
Start	31619725:31619725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1117G>A
AA Mutation	p.Glu373Lys(p.E373K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript