Colon Cancer: Gene >> CNNM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377075
Start	96762350:96762350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1351T>G
AA Mutation	p.Phe451Val(p.F451V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377075
Start	96797105:96797105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496T>C
AA Mutation	p.Val499Ala(p.V499A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377075
Start	96761966:96761966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367842804
CDS Mutation	c.967C>T
AA Mutation	p.Leu323Phe(p.L323F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377075
Start	96761702:96761702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703A>G
AA Mutation	p.Ile235Val(p.I235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000377075
Start	96797012:96797012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1403G>A
AA Mutation	p.Gly468Glu(p.G468E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377075
Start	96797625:96797625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763026644
CDS Mutation	c.1659C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377075
Start	96762305:96762306(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs768784550
CDS Mutation	c.1312dupC
AA Mutation	p.Leu438ProfsTer9(p.L438Pfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> CNNM4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377075
Start	96762092:96762092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1093G>T
AA Mutation	p.Ala365Ser(p.A365S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript