Colon Cancer: Gene >> LCMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43328587:43328587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1903C>T
AA Mutation	p.Pro635Ser(p.P635S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43330068:43330068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422G>A
AA Mutation	p.Arg141Lys(p.R141K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43329474:43329474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1016G>A
AA Mutation	p.Gly339Glu(p.G339E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43329316:43329316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1174C>T
AA Mutation	p.Leu392Phe(p.L392F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43329238:43329238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140361318
CDS Mutation	c.1252C>T
AA Mutation	p.Leu418Phe(p.L418F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305641
Start	43329563:43329563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000305641
Start	43329134:43329134(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1356delT
AA Mutation	p.Phe452LeufsTer11(p.F452Lfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> LCMT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305641
Start	43329639:43329639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305641
Start	43329446:43329446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780360954
CDS Mutation	c.1044C>T
Mutation Classification	Silent
Feature Type	Transcript