Colon Cancer: Gene >> CMTM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66609444:66609444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778469660
CDS Mutation	c.313C>T
AA Mutation	p.Arg105Cys(p.R105C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66609513:66609513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.382G>C
AA Mutation	p.Ala128Pro(p.A128P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66609943:66609943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777705777
CDS Mutation	c.460G>A
AA Mutation	p.Val154Met(p.V154M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66608351:66608351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.190G>A
AA Mutation	p.Ala64Thr(p.A64T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66608343:66608343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201311207
CDS Mutation	c.182C>T
AA Mutation	p.Ala61Val(p.A61V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66609495:66609495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372483559
CDS Mutation	c.364G>A
AA Mutation	p.Ala122Thr(p.A122T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CMTM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361909
Start	66608328:66608328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167T>G
AA Mutation	p.Phe56Cys(p.F56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript