Colon Cancer: Gene >> LCTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66563599:66563599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113055189
CDS Mutation	c.397G>A
AA Mutation	p.Glu133Lys(p.E133K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66551844:66551844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1342A>C
AA Mutation	p.Asn448His(p.N448H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66553154:66553154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027C>A
AA Mutation	p.His343Asn(p.H343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66563968:66563968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139752404
CDS Mutation	c.313G>A
AA Mutation	p.Val105Ile(p.V105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66564717:66564717(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.241G>A
AA Mutation	p.Glu81Lys(p.E81K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66557856:66557856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.788A>T
AA Mutation	p.Asp263Val(p.D263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341509
Start	66561039:66561039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529701551
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341509
Start	66548574:66548574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764784200
CDS Mutation	c.1620G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341509
Start	66563927:66563927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758343581
CDS Mutation	c.354G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000341509
Start	66563914:66563914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs539441696
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Ter(p.R123*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> LCTL

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66557997:66557997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376250011
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Cys(p.R249C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341509
Start	66553088:66553088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093G>A
AA Mutation	p.Asp365Asn(p.D365N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript