Colon Cancer: Gene >> TOP1MT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143325479:143325479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>C
AA Mutation	p.Asp180His(p.D180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143325493:143325493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.524G>T
AA Mutation	p.Gly175Val(p.G175V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143329433:143329433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200830353
CDS Mutation	c.277G>A
AA Mutation	p.Ala93Thr(p.A93T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000329245
Start	143334740:143334740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>A
AA Mutation	p.Arg41Lys(p.R41K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143317726:143317726(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776857154
CDS Mutation	c.1327C>T
AA Mutation	p.Arg443Cys(p.R443C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143324609:143324609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>T
AA Mutation	p.Pro231Leu(p.P231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143310197:143310197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1574G>A
AA Mutation	p.Arg525Gln(p.R525Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143321344:143321344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1003G>A
AA Mutation	p.Ala335Thr(p.A335T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143325419:143325419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146761712
CDS Mutation	c.598C>T
AA Mutation	p.Arg200Cys(p.R200C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329245
Start	143321231:143321231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1116C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329245
Start	143315768:143315768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748360764
CDS Mutation	c.1512G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TOP1MT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329245
Start	143318051:143318051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1182G>T
AA Mutation	p.Lys394Asn(p.K394N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript