Colon Cancer: Gene >> PDCL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295645
Start	55569854:55569854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756587149
CDS Mutation	c.226C>T
AA Mutation	p.Arg76Trp(p.R76W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295645
Start	55580862:55580862(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.177T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295645
Start	55556626:55556626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372967927
CDS Mutation	c.657A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295645
Start	55569762:55569762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PDCL2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000295645
Start	55569818:55569818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262A>C
AA Mutation	p.Lys88Gln(p.K88Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000295645
Start	55582193:55582193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780180638
CDS Mutation	c.51C>T
Mutation Classification	Silent
Feature Type	Transcript