Colon Cancer: Gene >> NSMF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371475
Start	137449419:137449419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1568T>C
AA Mutation	p.Leu523Pro(p.L523P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371475
Start	137457806:137457806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756007746
CDS Mutation	c.229G>A
AA Mutation	p.Gly77Ser(p.G77S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371475
Start	137449621:137449621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371475
Start	137452563:137452563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1155G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371475
Start	137457804:137457804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000371475
Start	137450020:137450020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1322G>A
AA Mutation	p.Trp441Ter(p.W441*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371475
Start	137457838:137457839(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.196dupC
AA Mutation	p.Gln66ProfsTer25(p.Q66Pfs*25)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NSMF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371475
Start	137453088:137453088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755038279
CDS Mutation	c.1015G>A
AA Mutation	p.Asp339Asn(p.D339N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371475
Start	137449450:137449450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372063291
CDS Mutation	c.1537C>T
AA Mutation	p.Arg513Cys(p.R513C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript