Colon Cancer: Gene >> PHOX2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41746301:41746301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.451G>A
AA Mutation	p.Ala151Thr(p.A151T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41747423:41747423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.355G>A
AA Mutation	p.Glu119Lys(p.E119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41747479:41747479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.299G>A
AA Mutation	p.Arg100His(p.R100H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41747372:41747372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>A
AA Mutation	p.Asp136Asn(p.D136N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41748526:41748526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>A
AA Mutation	p.Ala29Thr(p.A29T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41746279:41746279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.473G>A
AA Mutation	p.Arg158His(p.R158H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41747491:41747491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.287G>A
AA Mutation	p.Arg96His(p.R96H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41748381:41748381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.230C>T
AA Mutation	p.Pro77Leu(p.P77L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226382
Start	41748377:41748377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs73810366
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226382
Start	41746122:41746122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PHOX2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41746292:41746292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460C>T
AA Mutation	p.Arg154Cys(p.R154C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41747507:41747507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>A
AA Mutation	p.Gly91Ser(p.G91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226382
Start	41748405:41748405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.206C>A
AA Mutation	p.Thr69Asn(p.T69N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript