Colon Cancer: Gene >> NMBR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000258042
Start	142088639:142088639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.20C>A
AA Mutation	p.Ser7Tyr(p.S7Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000258042
Start	142078896:142078896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.430G>T
AA Mutation	p.Ala144Ser(p.A144S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000258042
Start	142078730:142078730(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.596T>C
AA Mutation	p.Ile199Thr(p.I199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000258042
Start	142088397:142088397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262G>A
AA Mutation	p.Gly88Arg(p.G88R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000258042
Start	142088532:142088532(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.127C>T
AA Mutation	p.Arg43Cys(p.R43C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258042
Start	142088242:142088242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747270958
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258042
Start	142078600:142078600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141034367
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258042
Start	142088281:142088281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.378C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258042
Start	142075672:142075672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NMBR

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000258042
Start	142075777:142075777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044G>A
Mutation Classification	Silent
Feature Type	Transcript