Colon Cancer: Gene >> CSHL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309894
Start	63910769:63910769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166G>C
AA Mutation	p.Glu56Gln(p.E56Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000309894
Start	63910452:63910452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147070430
CDS Mutation	c.274T>C
AA Mutation	p.Ser92Pro(p.S92P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000309894
Start	63910802:63910802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.133C>T
AA Mutation	p.Arg45Cys(p.R45C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000309894
Start	63910807:63910807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368141351
CDS Mutation	c.128C>T
AA Mutation	p.Ala43Val(p.A43V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309894
Start	63910285:63910285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139934003
CDS Mutation	c.348G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309894
Start	63910456:63910456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765806238
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000309894
Start	63910848:63910848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754967967
CDS Mutation	c.87C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CSHL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000309894
Start	63910269:63910269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374469041
CDS Mutation	c.364C>T
AA Mutation	p.Arg122Trp(p.R122W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript