Colon Cancer: Gene >> NEU4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391969
Start	241816749:241816749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs537701318
CDS Mutation	c.1156C>T
AA Mutation	p.Arg386Cys(p.R386C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391969
Start	241815057:241815057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370244576
CDS Mutation	c.367C>T
AA Mutation	p.Arg123Cys(p.R123C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000391969
Start	241816907:241816907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1314G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000391969
Start	241816407:241816408(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.815_819dupCTGCC
AA Mutation	p.Trp274LeufsTer51(p.W274Lfs*51)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NEU4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000391969
Start	241816273:241816273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374258246
CDS Mutation	c.680C>T
AA Mutation	p.Ala227Val(p.A227V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000391969
Start	241816188:241816188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377551488
CDS Mutation	c.595G>A
AA Mutation	p.Ala199Thr(p.A199T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000391969
Start	241814527:241814527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.43C>T
AA Mutation	p.Arg15Trp(p.R15W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript