Colon Cancer: Gene >> ST6GAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000169298
Start	187074185:187074185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.831C>A
AA Mutation	p.Phe277Leu(p.F277L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000169298
Start	187042891:187042891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.188T>C
AA Mutation	p.Val63Ala(p.V63A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000169298
Start	187051329:187051329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750567016
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Cys(p.R230C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000169298
Start	187072938:187072938(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000169298
Start	187075744:187075744(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1162G>T
AA Mutation	p.Glu388Ter(p.E388*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST6GAL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000169298
Start	187043295:187043295(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.592C>G
AA Mutation	p.Leu198Val(p.L198V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000169298
Start	187075677:187075677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750161610
CDS Mutation	c.1095G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000169298
Start	187074311:187074311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377592687
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript