Colon Cancer: Gene >> MTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150659734:150659734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1331G>A
AA Mutation	p.Cys444Tyr(p.C444Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150645788:150645788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781893456
CDS Mutation	c.784G>A
AA Mutation	p.Asp262Asn(p.D262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150619075:150619075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380G>A
AA Mutation	p.Gly127Asp(p.G127D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150638994:150638994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Val166Ile(p.V166I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150663556:150663556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1591T>G
AA Mutation	p.Leu531Val(p.L531V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370396
Start	150649838:150649838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370396
Start	150649811:150649811(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.969delA
AA Mutation	p.Val324Ter(p.V324*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370396
Start	150649810:150649811(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.969dupA
AA Mutation	p.Val324SerfsTer8(p.V324Sfs*8)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MTM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370396
Start	150663551:150663551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782468721
CDS Mutation	c.1586G>A
AA Mutation	p.Arg529His(p.R529H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript