Colon Cancer: Gene >> NXN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	826021:826021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418G>A
AA Mutation	p.Ala140Thr(p.A140T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	801031:801031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1226A>G
AA Mutation	p.Asp409Gly(p.D409G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	823640:823640(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201764402
CDS Mutation	c.604G>A
AA Mutation	p.Ala202Thr(p.A202T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	805208:805208(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.860T>C
AA Mutation	p.Val287Ala(p.V287A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	823644:823644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600C>A
AA Mutation	p.Phe200Leu(p.F200L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	823715:823715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Pro177Ser(p.P177S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336868
Start	819467:819467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.792G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336868
Start	819542:819542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs532150840
CDS Mutation	c.717G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336868
Start	805111:805111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777784278
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336868
Start	823659:823659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779780230
CDS Mutation	c.585C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NXN

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	825988:825988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451C>A
AA Mutation	p.Leu151Met(p.L151M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000336868
Start	803773:803773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1034A>C
AA Mutation	p.Lys345Thr(p.K345T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000336868
Start	819449:819449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs72810286
CDS Mutation	c.810C>T
Mutation Classification	Silent
Feature Type	Transcript