Colon Cancer: Gene >> B4GAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66347226:66347226(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.320T>A
AA Mutation	p.Leu107Gln(p.L107Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346104:66346104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1193G>A
AA Mutation	p.Arg398His(p.R398H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346228:66346228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069C>T
AA Mutation	p.His357Tyr(p.H357Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346234:66346234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063G>A
AA Mutation	p.Glu355Lys(p.E355K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346623:66346623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.923C>T
AA Mutation	p.Pro308Leu(p.P308L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66347253:66347253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.293C>G
AA Mutation	p.Ala98Gly(p.A98G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346750:66346750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.796C>T
AA Mutation	p.Arg266Cys(p.R266C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> B4GAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311181
Start	66346115:66346115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1182G>T
AA Mutation	p.Lys394Asn(p.K394N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311181
Start	66347186:66347186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360G>C
Mutation Classification	Silent
Feature Type	Transcript