Colon Cancer: Gene >> POLL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299206
Start	101579718:101579718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373860780
CDS Mutation	c.1463G>A
AA Mutation	p.Arg488His(p.R488H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299206
Start	101579463:101579463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1718G>A
AA Mutation	p.Arg573Gln(p.R573Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299206
Start	101586123:101586123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548269958
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299206
Start	101582832:101582832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41291484
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299206
Start	101584665:101584665(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> POLL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299206
Start	101586123:101586123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548269958
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299206
Start	101587280:101587280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81G>A
Mutation Classification	Silent
Feature Type	Transcript