Colon Cancer: Gene >> PENK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56445881:56445881(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Glu25Lys(p.E25K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56441777:56441777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299A>G
AA Mutation	p.Tyr100Cys(p.Y100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56441635:56441635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.441C>G
AA Mutation	p.Asp147Glu(p.D147E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56445848:56445848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106C>T
AA Mutation	p.Arg36Cys(p.R36C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314922
Start	56441440:56441440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000314922
Start	56441524:56441524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765857438
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PENK

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56441808:56441808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>T
AA Mutation	p.Pro90Ser(p.P90S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000314922
Start	56441450:56441450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626G>T
AA Mutation	p.Arg209Leu(p.R209L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript