Colon Cancer: Gene >> NETO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083707:47083707(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1092T>G
AA Mutation	p.Ile364Met(p.I364M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47109584:47109584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200233550
CDS Mutation	c.782A>G
AA Mutation	p.Asn261Ser(p.N261S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083523:47083523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772817589
CDS Mutation	c.1276C>T
AA Mutation	p.Arg426Trp(p.R426W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47128346:47128346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.460G>T
AA Mutation	p.Ala154Ser(p.A154S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083432:47083432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1367C>A
AA Mutation	p.Ser456Tyr(p.S456Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47083738:47083738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1061C>T
AA Mutation	p.Thr354Ile(p.T354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47083671:47083671(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47086278:47086278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.945C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47129327:47129327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.129C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000562435
Start	47128548:47128548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000562435
Start	47128484:47128484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.322C>T
AA Mutation	p.Arg108Ter(p.R108*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000562435
Start	47109549:47109549(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817C>T
AA Mutation	p.Arg273Ter(p.R273*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NETO2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000562435
Start	47128464:47128464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.342C>A
AA Mutation	p.Phe114Leu(p.F114L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript