Colon Cancer: Gene >> NRM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259953
Start	30689397:30689397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368813038
CDS Mutation	c.386G>A
AA Mutation	p.Arg129Gln(p.R129Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259953
Start	30689312:30689312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557071090
CDS Mutation	c.471C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259953
Start	30689414:30689414(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.369T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259953
Start	30690194:30690194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000259953
Start	30690921:30690921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.54C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000259953
Start	30690189:30690190(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.187dupC
AA Mutation	p.Leu63ProfsTer21(p.L63Pfs*21)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NRM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000259953
Start	30688875:30688875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.575T>C
AA Mutation	p.Phe192Ser(p.F192S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript