Colon Cancer: Gene >> ATN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936160:6936160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Thr298Ile(p.T298I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6935975:6935975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>T
AA Mutation	p.Lys236Asn(p.K236N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6937410:6937410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2143C>T
AA Mutation	p.Pro715Ser(p.P715S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936091:6936091(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201165264
CDS Mutation	c.824C>T
AA Mutation	p.Pro275Leu(p.P275L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6940885:6940885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3220G>A
AA Mutation	p.Ala1074Thr(p.A1074T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936465:6936465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1198C>T
AA Mutation	p.Pro400Ser(p.P400S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6936370:6936370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782462592
CDS Mutation	c.1103C>T
AA Mutation	p.Ala368Val(p.A368V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6935979:6935979(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.712G>C
AA Mutation	p.Gly238Arg(p.G238R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356654
Start	6941537:6941537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936491:6936491(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1228delC
AA Mutation	p.His410ThrfsTer43(p.H410Tfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936026:6936026(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.764delC
AA Mutation	p.Pro255HisfsTer43(p.P255Hfs*43)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000356654
Start	6936215:6936216(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.953dupC
AA Mutation	p.Gly319TrpfsTer61(p.G319Wfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> ATN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6941470:6941470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3455G>A
AA Mutation	p.Arg1152His(p.R1152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356654
Start	6937210:6937210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782754276
CDS Mutation	c.1943C>T
AA Mutation	p.Ala648Val(p.A648V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript