Colon Cancer: Gene >> NEU3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	75005579:75005579(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	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	74994715:74994715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Val101Ile(p.V101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	75005530:75005530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424G>T
AA Mutation	p.Gly142Cys(p.G142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	75005812:75005812(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371627063
CDS Mutation	c.706A>G
AA Mutation	p.Ile236Val(p.I236V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000294064
Start	74994573:74994573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.159A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEU3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	75005720:75005720(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.614G>C
AA Mutation	p.Gly205Ala(p.G205A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000294064
Start	74994646:74994646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.232C>G
AA Mutation	p.Arg78Gly(p.R78G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript