Colon Cancer: Gene >> PVR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425690
Start	44661800:44661800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1243G>T
AA Mutation	p.Gly415Cys(p.G415C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647344:44647344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745682626
CDS Mutation	c.201G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647269:44647269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44649897:44649897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377417539
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647282:44647282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.139C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647227:44647227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647530:44647530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.387G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44649948:44649948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150854789
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44649933:44649933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528582977
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000425690
Start	44647518:44647518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748886349
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PVR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000425690
Start	44658775:44658775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777036330
CDS Mutation	c.1025G>A
AA Mutation	p.Arg342His(p.R342H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript