Colon Cancer: Gene >> CREM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35148382:35148382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.59A>G
AA Mutation	p.Glu20Gly(p.E20G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35206943:35206943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647C>T
AA Mutation	p.Ala216Val(p.A216V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35148441:35148441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.118G>A
AA Mutation	p.Ala40Thr(p.A40T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35211686:35211686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786G>T
AA Mutation	p.Lys262Asn(p.K262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35188203:35188203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.413C>T
AA Mutation	p.Ala138Val(p.A138V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000345491
Start	35211675:35211675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770911193
CDS Mutation	c.775C>T
AA Mutation	p.Arg259Ter(p.R259*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CREM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345491
Start	35211748:35211748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.848T>A
AA Mutation	p.Leu283His(p.L283H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript