Colon Cancer: Gene >> CALU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249364
Start	128759809:128759809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600A>G
AA Mutation	p.Ile200Met(p.I200M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249364
Start	128769129:128769129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910G>T
AA Mutation	p.Asp304Tyr(p.D304Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249364
Start	128748614:128748614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.31T>A
AA Mutation	p.Ser11Thr(p.S11T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249364
Start	128748703:128748703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.120T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249364
Start	128748778:128748778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.195A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000249364
Start	128767512:128767512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.700C>T
AA Mutation	p.Arg234Ter(p.R234*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CALU

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249364
Start	128754370:128754370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330G>T
AA Mutation	p.Glu110Asp(p.E110D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript