Colon Cancer: Gene >> NEU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034524:233034524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138984578
CDS Mutation	c.610C>T
AA Mutation	p.Arg204Cys(p.R204C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034724:233034724(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.810G>T
AA Mutation	p.Gln270His(p.Q270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233032831:233032831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.160C>A
AA Mutation	p.Leu54Met(p.L54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034864:233034864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.950C>T
AA Mutation	p.Ala317Val(p.A317V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034575:233034575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.661G>A
AA Mutation	p.Val221Met(p.V221M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034525:233034525(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765031026
CDS Mutation	c.611G>A
AA Mutation	p.Arg204His(p.R204H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034852:233034852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376559802
CDS Mutation	c.938C>T
AA Mutation	p.Pro313Leu(p.P313L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034459:233034459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs2233393
CDS Mutation	c.545G>A
AA Mutation	p.Arg182Gln(p.R182Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034652:233034652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233034718:233034718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000233840
Start	233032737:233032737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> NEU2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000233840
Start	233034198:233034198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201616110
CDS Mutation	c.284C>T
AA Mutation	p.Thr95Met(p.T95M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript