Colon Cancer: Gene >> MTRF1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367233
Start	152998567:152998567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322A>T
AA Mutation	p.Thr108Ser(p.T108S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367233
Start	152989977:152989977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061A>T
AA Mutation	p.Tyr354Phe(p.Y354F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367233
Start	152990040:152990040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.998G>A
AA Mutation	p.Arg333Gln(p.R333Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367233
Start	152990072:152990072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.966G>T
AA Mutation	p.Glu322Asp(p.E322D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367233
Start	152990012:152990012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367233
Start	152994643:152994643(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.557delG
AA Mutation	p.Gly186ValfsTer8(p.G186Vfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000367233
Start	152990058:152990059(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.979_980insTTGGGAA
AA Mutation	p.Tyr327PhefsTer4(p.Y327Ffs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTRF1L

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367233
Start	152990048:152990048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990A>G
Mutation Classification	Silent
Feature Type	Transcript