Colon Cancer: Gene >> B3GNT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000622824
Start	77039573:77039573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.22T>C
AA Mutation	p.Ser8Pro(p.S8P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000622824
Start	77039600:77039600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>A
AA Mutation	p.Leu17Ile(p.L17I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000622824
Start	77040224:77040224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.673G>A
AA Mutation	p.Val225Met(p.V225M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622824
Start	77040238:77040238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622824
Start	77040217:77040217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622824
Start	77039662:77039662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.111G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000622824
Start	77039731:77039731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> B3GNT6

No Mutation Annotation!