Colon Cancer: Gene >> TBL1XR1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177050527:177050527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.511G>A
AA Mutation	p.Glu171Lys(p.E171K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177051644:177051644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287A>C
AA Mutation	p.Gln96Pro(p.Q96P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177038112:177038112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1108G>T
AA Mutation	p.Asp370Tyr(p.D370Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177033086:177033086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1301G>A
AA Mutation	p.Cys434Tyr(p.C434Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177051594:177051594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Ala113Thr(p.A113T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177050124:177050124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575C>T
AA Mutation	p.Thr192Ile(p.T192I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177046171:177046171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>A
AA Mutation	p.Ala295Thr(p.A295T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177047524:177047524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728G>T
AA Mutation	p.Gly243Val(p.G243V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177034265:177034265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1183T>C
AA Mutation	p.Tyr395His(p.Y395H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177038112:177038112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1108G>A
AA Mutation	p.Asp370Asn(p.D370N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177050016:177050016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.683T>C
AA Mutation	p.Val228Ala(p.V228A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000430069
Start	177051561:177051561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.370G>A
AA Mutation	p.Ala124Thr(p.A124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430069
Start	177025504:177025504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430069
Start	177047318:177047318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.846A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000430069
Start	177034271:177034271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000430069
Start	177051559:177051560(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.371_372insCCCGAATTAAAAGTTTA
AA Mutation	p.Lys125ProfsTer3(p.K125Pfs*3)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TBL1XR1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000430069
Start	177034271:177034271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1177G>T
AA Mutation	p.Glu393Ter(p.E393*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript