Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ST6GALNAC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76626327:76626327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377G>T
AA Mutation	p.Met459Ile(p.M459I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76629668:76629668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.175C>A
AA Mutation	p.Leu59Met(p.L59M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76627218:76627218(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548273650
CDS Mutation	c.1021C>T
AA Mutation	p.Arg341Cys(p.R341C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76629682:76629682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161G>T
AA Mutation	p.Arg54Met(p.R54M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76626687:76626687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1275G>T
AA Mutation	p.Leu425Phe(p.L425F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ST6GALNAC1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76629112:76629112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754834765
CDS Mutation	c.731C>T
AA Mutation	p.Thr244Met(p.T244M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000156626
Start	76643616:76643616(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23G>A
AA Mutation	p.Cys8Tyr(p.C8Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000156626
Start	76627170:76627171(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1068dupC
AA Mutation	p.Ala357ArgfsTer42(p.A357Rfs*42)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript