Colon Cancer: Gene >> GCNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502701:76502701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142199715
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76503216:76503216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs656106
CDS Mutation	c.835G>A
AA Mutation	p.Glu279Lys(p.E279K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502842:76502842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461T>C
AA Mutation	p.Val154Ala(p.V154A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502917:76502917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536C>T
AA Mutation	p.Ala179Val(p.A179V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502472:76502472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369681886
CDS Mutation	c.91G>A
AA Mutation	p.Val31Ile(p.V31I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502736:76502736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502975:76502975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594C>A
AA Mutation	p.Asn198Lys(p.N198K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502527:76502527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146C>T
AA Mutation	p.Ala49Val(p.A49V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76503232:76503232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851C>A
AA Mutation	p.Ser284Tyr(p.S284Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376730
Start	76503248:76503248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376730
Start	76503197:76503197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.816C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376730
Start	76503230:76503231(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.849_850insA
AA Mutation	p.Ser284IlefsTer10(p.S284Ifs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000376730
Start	76503288:76503289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.913dupA
AA Mutation	p.Ile305AsnfsTer15(p.I305Nfs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GCNT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76503122:76503122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.741G>A
AA Mutation	p.Met247Ile(p.M247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376730
Start	76502626:76502626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245T>G
AA Mutation	p.Phe82Cys(p.F82C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript