Colon Cancer: Gene >> NAAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75940811:75940811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75940078:75940078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294G>T
AA Mutation	p.Glu98Asp(p.E98D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75936175:75936175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.432G>T
AA Mutation	p.Leu144Phe(p.L144F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75925782:75925782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772892418
CDS Mutation	c.619G>A
AA Mutation	p.Ala207Thr(p.A207T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75919968:75919968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910G>A
AA Mutation	p.Ala304Thr(p.A304T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75919917:75919917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.961C>A
AA Mutation	p.Leu321Ile(p.L321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75940088:75940088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.284T>C
AA Mutation	p.Phe95Ser(p.F95S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75925769:75925769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.632G>A
AA Mutation	p.Arg211Gln(p.R211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NAAA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286733
Start	75919960:75919960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.918G>T
AA Mutation	p.Lys306Asn(p.K306N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript