Colon Cancer: Gene >> CABYR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24156373:24156373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.872T>C
AA Mutation	p.Val291Ala(p.V291A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24156723:24156723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1222G>A
AA Mutation	p.Ala408Thr(p.A408T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24143152:24143152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38G>A
AA Mutation	p.Gly13Asp(p.G13D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24156879:24156879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1378C>T
AA Mutation	p.His460Tyr(p.H460Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24143383:24143383(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169G>T
AA Mutation	p.Asp57Tyr(p.D57Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24156538:24156538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1037C>T
AA Mutation	p.Ser346Phe(p.S346F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463087
Start	24156011:24156011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000463087
Start	24156029:24156029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.528T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000463087
Start	24156252:24156252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.751G>T
AA Mutation	p.Glu251Ter(p.E251*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000463087
Start	24155754:24155754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.253G>T
AA Mutation	p.Glu85Ter(p.E85*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CABYR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24156673:24156673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1172C>T
AA Mutation	p.Ser391Phe(p.S391F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000463087
Start	24155735:24155735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.234G>T
AA Mutation	p.Lys78Asn(p.K78N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript