Colon Cancer: Gene >> NEU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31862127:31862127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.224A>G
AA Mutation	p.Asp75Gly(p.D75G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31861400:31861400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403G>A
AA Mutation	p.Asp135Asn(p.D135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31859898:31859898(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772426069
CDS Mutation	c.1069C>T
AA Mutation	p.Arg357Trp(p.R357W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31860224:31860224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839G>A
AA Mutation	p.Arg280Gln(p.R280Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31862037:31862037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>C
AA Mutation	p.Gly105Ala(p.G105A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31862094:31862094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.257C>T
AA Mutation	p.Pro86Leu(p.P86L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375631
Start	31862093:31862093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.258G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375631
Start	31862078:31862078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000375631
Start	31861203:31861203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750311018
CDS Mutation	c.600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000375631
Start	31860623:31860623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NEU1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31860150:31860150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761724054
CDS Mutation	c.913C>T
AA Mutation	p.Arg305Cys(p.R305C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000375631
Start	31862038:31862038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.313G>T
AA Mutation	p.Gly105Trp(p.G105W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript