Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ST3GAL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98785000:98785000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391A>G
AA Mutation	p.Thr131Ala(p.T131A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98793738:98793738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139832763
CDS Mutation	c.973G>A
AA Mutation	p.Val325Ile(p.V325I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98788399:98788399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>A
AA Mutation	p.Pro231His(p.P231H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98784993:98784993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.384G>T
AA Mutation	p.Lys128Asn(p.K128N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98784998:98784998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.389A>G
AA Mutation	p.Lys130Arg(p.K130R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000394162
Start	98788098:98788098(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.499delT
AA Mutation	p.Tyr167IlefsTer18(p.Y167Ifs*18)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000394162
Start	98773931:98773931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761826510
CDS Mutation	c.283C>T
AA Mutation	p.Arg95Ter(p.R95*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000394162
Start	98768429:98768429(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.-11-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> ST3GAL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98788445:98788445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.738A>T
AA Mutation	p.Lys246Asn(p.K246N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98788333:98788333(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.626A>C
AA Mutation	p.Asn209Thr(p.N209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000394162
Start	98793738:98793738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.973G>T
AA Mutation	p.Val325Leu(p.V325L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394162
Start	98788048:98788048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.444T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000394162
Start	98788150:98788150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747652874
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000394162
Start	98788109:98788109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>T
AA Mutation	p.Glu169Ter(p.E169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript