Colon Cancer: Gene >> CPT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50577005:50577005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs571187466
CDS Mutation	c.311G>A
AA Mutation	p.Arg104Gln(p.R104Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50571217:50571217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1816C>T
AA Mutation	p.Arg606Cys(p.R606C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50572034:50572034(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1547C>T
AA Mutation	p.Thr516Ile(p.T516I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50571240:50571240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745866439
CDS Mutation	c.1793G>A
AA Mutation	p.Arg598Gln(p.R598Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50574524:50574524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141802871
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50574539:50574539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.839C>T
AA Mutation	p.Ala280Val(p.A280V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50577864:50577864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760342156
CDS Mutation	c.52G>A
AA Mutation	p.Gly18Arg(p.G18R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50570313:50570313(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757184617
CDS Mutation	c.2122G>A
AA Mutation	p.Ala708Thr(p.A708T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50572032:50572032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773375016
CDS Mutation	c.1549C>T
AA Mutation	p.Arg517Trp(p.R517W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50572986:50572986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757229551
CDS Mutation	c.1241G>A
AA Mutation	p.Arg414His(p.R414H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50569625:50569625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2186A>G
AA Mutation	p.Glu729Gly(p.E729G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50574412:50574412(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Ala298Val(p.A298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312108
Start	50569382:50569382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2275C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312108
Start	50574541:50574541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.837C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000312108
Start	50570960:50570960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1959C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CPT1B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000312108
Start	50574524:50574524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141802871
CDS Mutation	c.854G>A
AA Mutation	p.Arg285His(p.R285H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript